{
    "batchid": 7,
    "recordid": "Q04446-1",
    "recordtype": "protein",
    "sections": {
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs748484690",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748484690"
                    },
                    {
                        "id": "rs748484690",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748484690"
                    },
                    {
                        "id": "rs748484690",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs748484690#frequency_tab"
                    },
                    {
                        "id": "rs748484690",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs748484690"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 522,
                "end_pos": 522,
                "sequence_org": "M",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577977",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M522",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703671781",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703671781"
                    },
                    {
                        "id": "rs1703671781",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703671781#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 522,
                "end_pos": 522,
                "sequence_org": "M",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577979",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M522",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs377162168",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377162168"
                    },
                    {
                        "id": "rs377162168",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377162168"
                    },
                    {
                        "id": "rs377162168",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs377162168#frequency_tab"
                    },
                    {
                        "id": "rs377162168",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs377162168"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 523,
                "end_pos": 523,
                "sequence_org": "I",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577976",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I523",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs377162168",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377162168"
                    },
                    {
                        "id": "rs377162168",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377162168"
                    },
                    {
                        "id": "rs377162168",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs377162168#frequency_tab"
                    },
                    {
                        "id": "rs377162168",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs377162168"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 523,
                "end_pos": 523,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577976",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I523",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs137852888",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852888"
                    },
                    {
                        "id": "rs137852888",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852888"
                    },
                    {
                        "id": "rs137852888",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs137852888#frequency_tab"
                    },
                    {
                        "id": "rs137852888",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs137852888"
                    },
                    {
                        "id": "15452297",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/15452297"
                    },
                    {
                        "id": "8613547",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/8613547"
                    },
                    {
                        "id": "rs137852888",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs137852888"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "subjects_tested": "3601",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "*",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577973",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3451",
                            "DOID:3149"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs137852888",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852888"
                    },
                    {
                        "id": "rs137852888",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852888"
                    },
                    {
                        "id": "rs137852888",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs137852888#frequency_tab"
                    },
                    {
                        "id": "rs137852888",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs137852888"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "sequence_org": "R",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577973",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs="
                    },
                    {
                        "id": "",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v="
                    },
                    {
                        "id": "rs80338673",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80338673"
                    },
                    {
                        "id": "rs80338673",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80338673"
                    },
                    {
                        "id": "rs80338673",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs80338673"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "subjects_tested": "3601",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577972",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs774619760",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774619760"
                    },
                    {
                        "id": "rs774619760",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774619760"
                    },
                    {
                        "id": "rs774619760",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774619760"
                    },
                    {
                        "id": "rs80338673",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80338673"
                    },
                    {
                        "id": "rs80338673",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80338673"
                    },
                    {
                        "id": "rs80338673",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs80338673"
                    },
                    {
                        "id": "10545044",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/10545044"
                    },
                    {
                        "id": "10762170",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/10762170"
                    },
                    {
                        "id": "15452297",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/15452297"
                    },
                    {
                        "id": "rs80338673",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs80338673"
                    },
                    {
                        "id": "rs774619760",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs774619760"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "subjects_tested": "1906",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577972",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "disease": [
                    {
                        "disease_id": "DOID:11054",
                        "recommended_name": {
                            "id": "DOID:11054",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11054",
                            "name": "urinary bladder cancer",
                            "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:11054",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:11054",
                                "name": "bladder cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:11054",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:11054",
                                "name": "tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the bladder."
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "tumour of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "bladder cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "cancer of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm, bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm, urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor, urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant tumour",
                                "description": ""
                            },
                            {
                                "id": "MIM:109800",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/109800",
                                "name": "Bladder cancer",
                                "description": "Bladder cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "11054",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:11054"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:5166",
                            "DOID:4114",
                            "DOID:2021",
                            "DOID:9460"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs552094593",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs552094593#frequency_tab"
                    },
                    {
                        "id": "rs552094593",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs552094593"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537021",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2471722837",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2471722837"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 524,
                "end_pos": 524,
                "sequence_org": "R",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577975",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R524",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703671092",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703671092"
                    },
                    {
                        "id": "rs1703671092",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703671092#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 526,
                "end_pos": 526,
                "sequence_org": "I",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577966",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I526",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs368248959",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs368248959"
                    },
                    {
                        "id": "rs368248959",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs368248959"
                    },
                    {
                        "id": "rs368248959",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs368248959#frequency_tab"
                    },
                    {
                        "id": "rs368248959",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs368248959"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 526,
                "end_pos": 526,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577967",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I526",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs745507588",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745507588"
                    },
                    {
                        "id": "rs745507588",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745507588"
                    },
                    {
                        "id": "rs745507588",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs745507588"
                    },
                    {
                        "id": "rs745507588",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs745507588"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 527,
                "end_pos": 527,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577964",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T527",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs780840389",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780840389"
                    },
                    {
                        "id": "rs780840389",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780840389"
                    },
                    {
                        "id": "rs780840389",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780840389"
                    },
                    {
                        "id": "rs780840389",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs780840389"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 527,
                "end_pos": 527,
                "subjects_tested": "4484",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "T",
                "sequence_mut": "M",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577963",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "T527",
                "disease": [
                    {
                        "disease_id": "DOID:1612",
                        "recommended_name": {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "breast cancer",
                            "description": "An organ system cancer that originates in the mammary gland."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "breast tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "malignant neoplasm of breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "malignant tumor of the breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "mammary cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "mammary tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:1612",
                                "name": "primary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma."
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer susceptibility, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, lobular, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of the breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, familial Male",
                                "description": ""
                            },
                            {
                                "id": "MIM:114480",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114480",
                                "name": "Breast cancer",
                                "description": "Breast cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3017",
                            "DOID:0050938"
                        ],
                        "evidence": [
                            {
                                "id": "1612",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1612"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1559650602",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1559650602"
                    },
                    {
                        "id": "rs1559650602",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1559650602"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 528,
                "end_pos": 528,
                "sequence_org": "H",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577960",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H528",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703670680",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703670680"
                    },
                    {
                        "id": "rs1703670680",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1703670680"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 529,
                "end_pos": 529,
                "sequence_org": "G",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577957",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G529",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs="
                    },
                    {
                        "id": "",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v="
                    }
                ],
                "glycoeffect": [],
                "start_pos": 529,
                "end_pos": 529,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "R",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577958",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "G529",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3451",
                            "DOID:3149"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 529,
                "end_pos": 529,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81577957",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "G529",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs="
                    },
                    {
                        "id": "",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v="
                    }
                ],
                "glycoeffect": [],
                "start_pos": 52,
                "end_pos": 52,
                "sequence_org": "F",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "NC_000003.12",
                "chr_pos": "81705603",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "F52",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2106933633",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2106933633"
                    },
                    {
                        "id": "rs2106933633",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2106933633"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 531,
                "end_pos": 531,
                "sequence_org": "G",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577951",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G531",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751331135",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751331135"
                    },
                    {
                        "id": "rs751331135",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751331135"
                    },
                    {
                        "id": "rs751331135",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs751331135#frequency_tab"
                    },
                    {
                        "id": "rs751331135",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751331135"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 531,
                "end_pos": 531,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577952",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G531",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703670495",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703670495"
                    },
                    {
                        "id": "rs1703670495",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703670495"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 534,
                "end_pos": 534,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577943",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G534",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2106933621",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2106933621"
                    },
                    {
                        "id": "rs2106933621",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2106933621"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 534,
                "end_pos": 534,
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577942",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G534",
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2471722766",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2471722766"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 535,
                "end_pos": 535,
                "sequence_org": "Y",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577938",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y535",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs886058900",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs886058900"
                    },
                    {
                        "id": "rs886058900",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs886058900#frequency_tab"
                    },
                    {
                        "id": "rs886058900",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs886058900"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 535,
                "end_pos": 535,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577939",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y535",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703670422",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703670422"
                    },
                    {
                        "id": "rs1703670422",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1703670422"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 536,
                "end_pos": 536,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577937",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L536",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs="
                    },
                    {
                        "id": "",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v="
                    }
                ],
                "glycoeffect": [],
                "start_pos": 538,
                "end_pos": 538,
                "sequence_org": "F",
                "sequence_mut": "S",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "NC_000003.12",
                "chr_pos": "81536978",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "F538",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1319283898",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1319283898"
                    },
                    {
                        "id": "rs1319283898",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1319283898"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 538,
                "end_pos": 538,
                "sequence_org": "F",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577931",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F538",
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703670363",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703670363"
                    },
                    {
                        "id": "rs1703670363",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703670363#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 539,
                "end_pos": 539,
                "sequence_org": "M",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577928",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M539",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1245333229",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1245333229"
                    },
                    {
                        "id": "rs1245333229",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1245333229#frequency_tab"
                    },
                    {
                        "id": "rs1245333229",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1245333229"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 53,
                "end_pos": 53,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81705598",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S53",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1168126093",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1168126093"
                    },
                    {
                        "id": "rs1168126093",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1168126093"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 540,
                "end_pos": 540,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81577925",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G540",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703086906",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086906"
                    },
                    {
                        "id": "rs1703086906",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703086906#frequency_tab"
                    },
                    {
                        "id": "rs1703086906",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703086906"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 541,
                "end_pos": 541,
                "sequence_org": "N",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537093",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N541",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2471675648",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2471675648"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 541,
                "end_pos": 541,
                "sequence_org": "N",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537092",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N541",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703086906",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086906"
                    },
                    {
                        "id": "rs1703086906",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703086906#frequency_tab"
                    },
                    {
                        "id": "rs1703086906",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703086906"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 541,
                "end_pos": 541,
                "sequence_org": "N",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537093",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N541",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 543,
                "end_pos": 543,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "F",
                "sequence_mut": "C",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537086",
                "ref_nt": "A",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "F543",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 544,
                "end_pos": 544,
                "subjects_tested": "4177",
                "subjects_positive": "2",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "E",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537083",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "G544",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer susceptibility, X-linked",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "Prca1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "predisposing for prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, on chromosome 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer aggressiveness",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs137852889",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852889"
                    },
                    {
                        "id": "rs137852889",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs137852889"
                    },
                    {
                        "id": "15452297",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/15452297"
                    },
                    {
                        "id": "8247964",
                        "database": "PubMed",
                        "url": ""
                    }
                ],
                "glycoeffect": [],
                "start_pos": 545,
                "end_pos": 545,
                "sequence_org": "H",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537080",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H545",
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1559637866",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1559637866"
                    },
                    {
                        "id": "rs1559637866",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1559637866"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 545,
                "end_pos": 545,
                "sequence_org": "H",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537081",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H545",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs564155033",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs564155033"
                    },
                    {
                        "id": "rs564155033",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs564155033"
                    },
                    {
                        "id": "rs564155033",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs564155033"
                    },
                    {
                        "id": "rs564155033",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs564155033"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 546,
                "end_pos": 546,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "P",
                "sequence_mut": "T",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537078",
                "ref_nt": "G",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "P546",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:5166",
                            "DOID:4114",
                            "DOID:2021",
                            "DOID:9460"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086549"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703086549#frequency_tab"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703086549"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1703086549"
                    },
                    {
                        "id": "rs137852894",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852894"
                    },
                    {
                        "id": "rs137852894",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137852894"
                    },
                    {
                        "id": "17662246",
                        "database": "PubMed",
                        "url": ""
                    }
                ],
                "glycoeffect": [],
                "start_pos": 548,
                "end_pos": 548,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "W",
                "sequence_mut": "*",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537070",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "W548",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:5166",
                            "DOID:4114",
                            "DOID:2021",
                            "DOID:9460"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703086549",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086549"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703086549#frequency_tab"
                    },
                    {
                        "id": "rs1703086549",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703086549"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 548,
                "end_pos": 548,
                "sequence_org": "W",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537070",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W548",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1056584942",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1056584942"
                    },
                    {
                        "id": "rs1056584942",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1056584942"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 549,
                "end_pos": 549,
                "sequence_org": "L",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537068",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L549",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs544404712",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs544404712"
                    },
                    {
                        "id": "rs544404712",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs544404712"
                    },
                    {
                        "id": "rs544404712",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs544404712#frequency_tab"
                    },
                    {
                        "id": "rs544404712",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs544404712"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 549,
                "end_pos": 549,
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537067",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000196232",
                "site_lbl": "L549",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2471917618",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2471917618"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 54,
                "end_pos": 54,
                "sequence_org": "Q",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81705595",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q54",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703086412",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086412"
                    },
                    {
                        "id": "rs1703086412",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1703086412"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 550,
                "end_pos": 550,
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537065",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D550",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703086329",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086329"
                    },
                    {
                        "id": "rs1703086329",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1703086329#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 551,
                "end_pos": 551,
                "sequence_org": "F",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537062",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F551",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 551,
                "end_pos": 551,
                "subjects_tested": "1773",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "F",
                "sequence_mut": "V",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537063",
                "ref_nt": "A",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "F551",
                "disease": [
                    {
                        "disease_id": "DOID:5041",
                        "recommended_name": {
                            "id": "DOID:5041",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Distal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Proximal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of the middle Third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the esophagus."
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal squamous cell carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "oesophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the middle third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of abdominal oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the middle third of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Aerodigestive tract cancer, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Escc, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal squamous cell carcinoma, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "gastric cardia adenocarcinoma, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MIM:133239",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/133239",
                                "name": "Esophageal cancer",
                                "description": "Esophageal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "5041",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:5041"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:10534",
                        "recommended_name": {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10534",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10534",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the stomach."
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca lesser curvature - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "GC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "cancer of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer risk after h. pylori infection",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant stomach neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "stomach cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca body - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "ca greater curvature of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, intestinal",
                                "description": ""
                            },
                            {
                                "id": "MIM:613659",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/613659",
                                "name": "Gastric cancer",
                                "description": "Gastric cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            },
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs777589783",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777589783"
                    },
                    {
                        "id": "rs777589783",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777589783"
                    },
                    {
                        "id": "rs777589783",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs777589783#frequency_tab"
                    },
                    {
                        "id": "rs777589783",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs777589783"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 552,
                "end_pos": 552,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537059",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P552",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs1703086279",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703086279"
                    },
                    {
                        "id": "rs1703086279",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1703086279"
                    },
                    {
                        "id": "rs1703086279",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1703086279"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 552,
                "end_pos": 552,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537060",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "P552",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3451",
                            "DOID:3149"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 553,
                "end_pos": 553,
                "subjects_tested": "1704",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "I",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537056",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R553",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:5166",
                            "DOID:4114",
                            "DOID:2021",
                            "DOID:9460"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs758472321",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs758472321"
                    },
                    {
                        "id": "rs758472321",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs758472321"
                    },
                    {
                        "id": "rs758472321",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs758472321"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 554,
                "end_pos": 554,
                "sequence_org": "K",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537053",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K554",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs937683680",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs937683680"
                    },
                    {
                        "id": "rs937683680",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs937683680#frequency_tab"
                    },
                    {
                        "id": "rs937683680",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs937683680"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 556,
                "end_pos": 556,
                "sequence_org": "N",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537048",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N556",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs937683680",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs937683680"
                    },
                    {
                        "id": "rs937683680",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs937683680#frequency_tab"
                    },
                    {
                        "id": "rs937683680",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs937683680"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 556,
                "end_pos": 556,
                "sequence_org": "N",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537048",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N556",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2471675503",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2471675503"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 558,
                "end_pos": 558,
                "sequence_org": "E",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537043",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E558",
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756270678",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756270678"
                    },
                    {
                        "id": "rs756270678",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756270678"
                    },
                    {
                        "id": "rs756270678",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756270678"
                    },
                    {
                        "id": "rs756270678",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs756270678"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 558,
                "end_pos": 558,
                "sequence_org": "E",
                "sequence_mut": "D",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537040",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E558",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs765212625",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765212625"
                    },
                    {
                        "id": "rs765212625",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765212625"
                    },
                    {
                        "id": "rs765212625",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs765212625"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 558,
                "end_pos": 558,
                "sequence_org": "E",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537042",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E558",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1703085718",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1703085718"
                    },
                    {
                        "id": "rs1703085718",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1703085718"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-loss",
                    "o-glyco-site-loss"
                ],
                "start_pos": 559,
                "end_pos": 559,
                "sequence_org": "S",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537038",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S559",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1412857849",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1412857849"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-loss",
                    "o-glyco-site-loss"
                ],
                "start_pos": 559,
                "end_pos": 559,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537039TC",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S559",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 55,
                "end_pos": 55,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "I",
                "sequence_mut": "L",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81705594",
                "ref_nt": "T",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "I55",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:5166",
                            "DOID:4114",
                            "DOID:2021",
                            "DOID:9460"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1559637815",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1559637815"
                    },
                    {
                        "id": "rs1559637815",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1559637815"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 560,
                "end_pos": 560,
                "sequence_org": "Y",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537034",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y560",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs770040230",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs770040230"
                    },
                    {
                        "id": "rs770040230",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs770040230"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 560,
                "end_pos": 560,
                "sequence_org": "Y",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537036",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y560",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs750478545",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs750478545"
                    },
                    {
                        "id": "rs750478545",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs750478545"
                    },
                    {
                        "id": "rs750478545",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs750478545"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 562,
                "end_pos": 562,
                "sequence_org": "Y",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537030",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y562",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1313202468",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1313202468"
                    },
                    {
                        "id": "rs1313202468",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1313202468"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 563,
                "end_pos": 563,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537026",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A563",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs767657413",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767657413"
                    },
                    {
                        "id": "rs767657413",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767657413"
                    },
                    {
                        "id": "rs767657413",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs767657413#frequency_tab"
                    },
                    {
                        "id": "rs767657413",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs767657413"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 564,
                "end_pos": 564,
                "sequence_org": "R",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537023",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R564",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 565,
                "end_pos": 565,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537020",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R565",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3451",
                            "DOID:3149"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs774619760",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774619760"
                    },
                    {
                        "id": "rs774619760",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774619760"
                    },
                    {
                        "id": "rs774619760",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774619760"
                    },
                    {
                        "id": "rs774619760",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs774619760"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 565,
                "end_pos": 565,
                "subjects_tested": "720",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537020",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "R565",
                "disease": [
                    {
                        "disease_id": "DOID:10534",
                        "recommended_name": {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10534",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:10534",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the stomach."
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca lesser curvature - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "GC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "cancer of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer risk after h. pylori infection",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant stomach neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "stomach cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca body - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "ca greater curvature of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, intestinal",
                                "description": ""
                            },
                            {
                                "id": "MIM:613659",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/613659",
                                "name": "Gastric cancer",
                                "description": "Gastric cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            },
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:5041",
                        "recommended_name": {
                            "id": "DOID:5041",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Distal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Proximal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of the middle Third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the esophagus."
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal squamous cell carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "oesophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the middle third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of abdominal oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the middle third of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Aerodigestive tract cancer, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Escc, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal squamous cell carcinoma, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "gastric cardia adenocarcinoma, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MIM:133239",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/133239",
                                "name": "Esophageal cancer",
                                "description": "Esophageal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "5041",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:5041"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "rs552094593",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs552094593#frequency_tab"
                    },
                    {
                        "id": "rs552094593",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs552094593"
                    },
                    {
                        "id": "rs552094593",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs552094593"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 565,
                "end_pos": 565,
                "subjects_tested": "4799",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537021",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R565",
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "Nonsmall cell lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "alveolar cell carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "adenocarcinoma of lung, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111375",
                        "recommended_name": {
                            "id": "DOID:0111375",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111375",
                            "name": "fetal akinesia deformation sequence syndrome",
                            "description": "A syndrome characterized by decreased fetal movements, intrauterine growth restriction, joint contractures, and developmental anomalies, including lung hypoplasia, cleft palate, and cryptorchidism that often has_material_basis_in mutation in a gene associated with the neuromuscular junction."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "FADS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "fetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia deformation sequence syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111375",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111375",
                                "name": "foetal akinesia sequence",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "208150",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/208150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111377",
                        "recommended_name": {
                            "id": "DOID:0111377",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0111377",
                            "name": "fetal akinesia deformation sequence syndrome 1",
                            "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the MUSK gene on chromosome 9q31.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111377",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0111377",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "fetal akinesia deformation sequence 1",
                                "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the MUSK gene."
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "FADS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0100101",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0100101",
                                "name": "Pena-Shokeir syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:208150",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/208150",
                                "name": "Fetal akinesia deformation sequence 1",
                                "description": "Fetal akinesia deformation sequence 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            },
                            {
                                "id": "0111377",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111377"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 567,
                "end_pos": 567,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "F",
                "sequence_mut": "L",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537015",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "F567",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1346550496",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1346550496"
                    },
                    {
                        "id": "rs1346550496",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1346550496"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 568,
                "end_pos": 568,
                "sequence_org": "H",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537011",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H568",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1346550496",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1346550496"
                    },
                    {
                        "id": "rs1346550496",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1346550496"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 568,
                "end_pos": 568,
                "sequence_org": "H",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537011",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H568",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "Q04446",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q04446"
                    },
                    {
                        "id": "",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs="
                    },
                    {
                        "id": "",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v="
                    }
                ],
                "glycoeffect": [],
                "start_pos": 569,
                "end_pos": 569,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "L",
                "sequence_mut": "*",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
                "chr_id": "3",
                "chr_pos": "81537008",
                "ref_nt": "A",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "L569",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "large intestine cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1204592637",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1204592637"
                    },
                    {
                        "id": "rs1204592637",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1204592637"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 56,
                "end_pos": 56,
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81705591",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L56",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs941646149",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs941646149"
                    },
                    {
                        "id": "rs941646149",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs941646149"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 571,
                "end_pos": 571,
                "sequence_org": "D",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "3",
                "chr_pos": "81537002",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D571",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2750",
                        "recommended_name": {
                            "id": "DOID:2750",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:2750",
                            "name": "glycogen storage disease IV",
                            "description": "A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "DOID:2750",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:2750",
                                "name": "Glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": "Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases."
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen Disease (GSD IV)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Andersen's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GBE1 glycogen storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "amylopectinosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "branching-transferase deficiency glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "deficiency of 1,4-alpha-glucan branching enzyme",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease caused by mutation in GBE1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease, type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis due to glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis type IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, classic hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, adult, with isolated myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, childhood",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, neuromuscular form, fatal perinatal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD IV, nonprogressive hepatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "GSD4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "Gbe1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "brancher deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "cirrhosis, familial, with deposition of abnormal glycogen",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen branching enzyme deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogen storage disease IV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009292",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009292",
                                "name": "glycogenosis 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:232500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/232500",
                                "name": "Glycogen storage disease 4",
                                "description": "Glycogen storage disease 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "232500",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/232500"
                            },
                            {
                                "id": "2750",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2750"
                            }
                        ]
                    }
                ]
            }
        ]
    }
}
