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                                "name": "GC",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009267"
                            },
                            {
                                "id": "231000",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/231000"
                            },
                            {
                                "id": "0110959",
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                            }
                        ]
                    },
                    {
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                            },
                            {
                                "id": "DOID:0110959",
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                                "description": ""
                            },
                            {
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                                "url": "http://disease-ontology.org/term/DOID:0110959",
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                                "description": ""
                            },
                            {
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                                "description": ""
                            },
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                            },
                            {
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                            },
                            {
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                                "description": ""
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
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                                "description": ""
                            },
                            {
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                                "description": ""
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, juvenile and adult, cerebral",
                                "description": ""
                            },
                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
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                                "description": ""
                            },
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                                "resource": "MONDO",
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                                "description": ""
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                            {
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                                "description": ""
                            },
                            {
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
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                                "description": ""
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                            {
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                                "resource": "MONDO",
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                            {
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                                "description": ""
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                            {
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                            {
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                                "description": ""
                            },
                            {
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                                "description": ""
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                            {
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                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/231000",
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                            {
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                    },
                    {
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                            {
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                            {
                                "id": "MONDO:0009268",
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                            },
                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
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                            {
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                            {
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                            {
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                            {
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                                "resource": "MONDO",
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                            {
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                            {
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                    },
                    {
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                            "url": "http://disease-ontology.org/term/DOID:0060892",
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                            {
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                                "resource": "MONDO",
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                            {
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                                "resource": "MONDO",
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                            },
                            {
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                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "LOPD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PARK",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, age of onset, modifier, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "autosomal dominant late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:168600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/168600",
                                "name": "Parkinson disease",
                                "description": "Parkinson disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "14330",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14330"
                            },
                            {
                                "id": "14330",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14330"
                            }
                        ]
                    }
                ],
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                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1219332583",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1219332583"
                    },
                    {
                        "id": "rs1219332583",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1219332583"
                    }
                ],
                "glycoeffect": [],
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                "end_pos": 316,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 0 out of 0 filters:",
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                "chr_pos": "155237393",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R316",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P04062",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04062"
                    },
                    {
                        "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": [],
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                "end_pos": 316,
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                "sequence_mut": "L",
                "comment": "All mutations pass selection filters for glycohydrolase proteins.",
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                "alt_nt": "A",
                "minor_allelic_frequency": "",
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                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:4159",
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                            "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": "",
                        "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": 319,
                "end_pos": 319,
                "sequence_org": "M",
                "sequence_mut": "V",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "NC_000001.11",
                "chr_pos": "155237385",
                "ref_nt": "T",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "M319",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1461588734",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1461588734"
                    },
                    {
                        "id": "rs1461588734",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1461588734"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 31,
                "end_pos": 31,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "1",
                "chr_pos": "155240654",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L31",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1276605197",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1276605197"
                    },
                    {
                        "id": "rs1276605197",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1276605197"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 321,
                "end_pos": 321,
                "sequence_org": "D",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "1",
                "chr_pos": "155237378",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D321",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1276605197",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1276605197"
                    },
                    {
                        "id": "rs1276605197",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1276605197"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 321,
                "end_pos": 321,
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 0 out of 0 filters:",
                "chr_id": "1",
                "chr_pos": "155237378",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D321",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2524830661",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2524830661"
                    },
                    {
                        "id": "rs2524830661",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs2524830661"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 322,
                "end_pos": 322,
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 0 out of 0 filters:",
                "chr_id": "1",
                "chr_pos": "155237376",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D322",
                "disease": [
                    {
                        "disease_id": "DOID:0110957",
                        "recommended_name": {
                            "id": "DOID:0110957",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0110957",
                            "name": "Gaucher's disease type I",
                            "description": "A Gaucher's disease characterized by absence of primary central nervous system involvement that has_material_basis_homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "Acid Beta-Glucosidase Deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "GD I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "Gaucher Disease, Noncerebral Juvenile",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "Gba Deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "Glucocerebrosidase Deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110957",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110957",
                                "name": "GD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease type I",
                                "description": "Gaucher disease type 1 is the chronic non-neurological form of Gaucher disease (GD) characterized by organomegaly, bone involvement and cytopenia."
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "GD I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease type I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease, noncerebral juvenile",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher's disease type I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gba deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "acid Beta-glucosidase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "non-cerebral juvenile Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gaucher disease, type I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265",
                                "name": "Gd 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:230800",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/230800",
                                "name": "Gaucher disease 1",
                                "description": "Gaucher disease 1"
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                        "evidence": [
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                                "id": "0009265",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009265"
                            },
                            {
                                "id": "230800",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/230800"
                            },
                            {
                                "id": "0110957",
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                            }
                        ]
                    }
                ],
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            },
            {
                "evidence": [
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                        "id": "P04062",
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                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04062"
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                ],
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                "site_lbl": "D322",
                "disease": [
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                        "disease_id": "DOID:9256",
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                            "resource": "Disease Ontology",
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                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
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                        "synonyms": [
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                                "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": ""
                            },
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, acute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
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                                "description": ""
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                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
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                            {
                                "id": "MONDO:0009266",
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                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
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                            },
                            {
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                                "description": ""
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                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
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                                "description": ""
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                            {
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                                "resource": "MIM",
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                            {
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                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": "Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1."
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Subacute neuronopathic type",
                                "description": ""
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, chronic neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, juvenile and adult, cerebral",
                                "description": ""
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, subacute neuronopathic type",
                                "description": ""
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                                "id": "MONDO:0009267",
                                "resource": "MONDO",
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                                "name": "Gaucher's disease type III",
                                "description": ""
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                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
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                                "description": ""
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                                "id": "MONDO:0009267",
                                "resource": "MONDO",
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                                "name": "Gaucher's disease type I",
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                            {
                                "id": "MONDO:0009265",
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                            {
                                "id": "MONDO:0009265",
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                            {
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                                "id": "MONDO:0009265",
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                            {
                                "id": "MONDO:0009265",
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                            {
                                "id": "MONDO:0009265",
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                            {
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                                "resource": "MONDO",
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                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
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                        },
                        "synonyms": [
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                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Chronic Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Juvenile And Adult, Cerebral",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Subacute Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": "Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1."
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Subacute neuronopathic type",
                                "description": ""
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, chronic neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, juvenile and adult, cerebral",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, subacute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher's disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "cerebral juvenile and adult form of Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "chronic neuronopathic Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Norrbottnian type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3A",
                                "description": ""
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3B",
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                            },
                            {
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                                "description": ""
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
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                                "description": ""
                            },
                            {
                                "id": "MIM:231000",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/231000",
                                "name": "Gaucher disease 3",
                                "description": "Gaucher disease 3"
                            }
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                            {
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                                "description": ""
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                            {
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                            {
                                "id": "MONDO:0009266",
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gd 2",
                                "description": ""
                            },
                            {
                                "id": "MIM:230900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/230900",
                                "name": "Gaucher disease 2",
                                "description": "Gaucher disease 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0009266",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266"
                            },
                            {
                                "id": "230900",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/230900"
                            },
                            {
                                "id": "0110958",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110958"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110958",
                        "recommended_name": {
                            "id": "DOID:0110958",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0110958",
                            "name": "Gaucher's disease type II",
                            "description": "A Gaucher's disease characterized by rapid neurologic deterioration with cranial nerve and extrapyramidal tract involvement that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110958",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110958",
                                "name": "GD II",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110958",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110958",
                                "name": "Gaucher Disease, Acute Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110958",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110958",
                                "name": "Infantile Cerebral Gaucher Disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110958",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110958",
                                "name": "GD2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease type II",
                                "description": "Gaucher disease type 2 is the acute neurological form of Gaucher disease (GD). It is characterized by early-onset and severe neurological involvement of the brainstem, associated with an organomegaly and generally leading to death before the age of 2."
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "GD II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, acute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher's disease type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "acute neuronopathic Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "infantile cerebral Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, infantile cerebral",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gaucher disease, type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009266",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266",
                                "name": "Gd 2",
                                "description": ""
                            },
                            {
                                "id": "MIM:230900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/230900",
                                "name": "Gaucher disease 2",
                                "description": "Gaucher disease 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0009266",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009266"
                            },
                            {
                                "id": "230900",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/230900"
                            },
                            {
                                "id": "0110958",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110958"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110959",
                        "recommended_name": {
                            "id": "DOID:0110959",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0110959",
                            "name": "Gaucher's disease type III",
                            "description": "A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Chronic Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Juvenile And Adult, Cerebral",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Subacute Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": "Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1."
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Subacute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, chronic neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, juvenile and adult, cerebral",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, subacute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher's disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "cerebral juvenile and adult form of Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "chronic neuronopathic Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Norrbottnian type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3A",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gd 3",
                                "description": ""
                            },
                            {
                                "id": "MIM:231000",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/231000",
                                "name": "Gaucher disease 3",
                                "description": "Gaucher disease 3"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0009267",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267"
                            },
                            {
                                "id": "231000",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/231000"
                            },
                            {
                                "id": "0110959",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110959"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110959",
                        "recommended_name": {
                            "id": "DOID:0110959",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0110959",
                            "name": "Gaucher's disease type III",
                            "description": "A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Chronic Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Juvenile And Adult, Cerebral",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110959",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0110959",
                                "name": "Gaucher Disease, Subacute Neuronopathic Type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": "Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1."
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "GD III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Subacute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, chronic neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, juvenile and adult, cerebral",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, subacute neuronopathic type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher's disease type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "cerebral juvenile and adult form of Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "chronic neuronopathic Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, Norrbottnian type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3A",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type 3B",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gaucher disease, type III",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009267",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267",
                                "name": "Gd 3",
                                "description": ""
                            },
                            {
                                "id": "MIM:231000",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/231000",
                                "name": "Gaucher disease 3",
                                "description": "Gaucher disease 3"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0009267",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009267"
                            },
                            {
                                "id": "231000",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/231000"
                            },
                            {
                                "id": "0110959",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110959"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0112250",
                        "recommended_name": {
                            "id": "DOID:0112250",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0112250",
                            "name": "Gaucher's disease type IIIC",
                            "description": "A Gaucher's disease type III characterized by additional presence of cardiovascular calcifications that has_material_basis_in homozygosity for an asp409-to-his (D409H) mutation in the GBA1 gene on chromosome 1q22."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "GD3C",
                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "Gaucher disease type 3C",
                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "Gaucher-like disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "cardiovascular Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome",
                                "description": "Gaucher disease - ophthalmoplegia - cardiovascular calcification is a variant of Gaucher disease, also known as a Gaucher-like disease that is characterized by cardiac involvement."
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher disease type 3C",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher-like disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "cardiovascular Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher disease - ophthalmoplegia - cardiovascular calcification",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
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                                "name": "Gaucher disease, type IIIC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "pseudo Gaucher disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:231005",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/231005",
                                "name": "Gaucher disease 3C",
                                "description": "Gaucher disease 3C"
                            }
                        ],
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                        "evidence": [
                            {
                                "id": "0009268",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268"
                            },
                            {
                                "id": "231005",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/231005"
                            },
                            {
                                "id": "0112250",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0112250"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0112250",
                        "recommended_name": {
                            "id": "DOID:0112250",
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                            "url": "http://disease-ontology.org/term/DOID:0112250",
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                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome",
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                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
                                "name": "GD3C",
                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0112250",
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                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
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                                "description": ""
                            },
                            {
                                "id": "DOID:0112250",
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                            },
                            {
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                            {
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                            },
                            {
                                "id": "MONDO:0009268",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
                                "name": "Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0009268",
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                            },
                            {
                                "id": "MONDO:0009268",
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                                "description": ""
                            },
                            {
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                            },
                            {
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                            },
                            {
                                "id": "MONDO:0009268",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0009268",
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                                "description": ""
                            },
                            {
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                                "resource": "MIM",
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                            {
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                            },
                            {
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                    },
                    {
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                                "description": ""
                            },
                            {
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                                "description": ""
                            },
                            {
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                                "description": ""
                            },
                            {
                                "id": "DOID:12217",
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                                "url": "http://disease-ontology.org/term/DOID:12217",
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                            {
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                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "DLB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Lewy body dementia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Lewy body disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Senile dementia of the Lewy body type",
                                "description": ""
                            },
                            {
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
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                                "description": ""
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                            {
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                                "description": ""
                            },
                            {
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "dementia, Lewy body",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "diffuse Lewy body disease with gaze palsy",
                                "description": ""
                            },
                            {
                                "id": "MIM:127750",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/127750",
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                                "description": "Dementia, Lewy body"
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                    },
                    {
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                        },
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                            {
                                "id": "DOID:12217",
                                "resource": "Disease Ontology",
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                                "description": ""
                            },
                            {
                                "id": "DOID:12217",
                                "resource": "Disease Ontology",
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                                "description": ""
                            },
                            {
                                "id": "DOID:12217",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:12217",
                                "name": "Senile dementia of the Lewy body type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
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                                "description": "A progressive form of dementia characterized by the presence of protein deposits called Lewy bodies in the midbrain and cerebral cortex, and loss of cholinergic and dopaminergic neurons. The signs and symptoms overlap with Alzheimer and Parkinson disease."
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "DLB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Lewy body dementia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Lewy body disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Senile dementia of the Lewy body type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "cortical Lewy body disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "dementia with Lewy bodies",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "lewy body dementia, susceptibility to",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "Lewy body variant of Alzheimer disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "dementia, Lewy body",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "diffuse Lewy body disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "diffuse Lewy body disease with gaze palsy",
                                "description": ""
                            },
                            {
                                "id": "MIM:127750",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/127750",
                                "name": "Dementia, Lewy body",
                                "description": "Dementia, Lewy body"
                            }
                        ],
                        "unlinked_id_list": [],
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                            {
                                "id": "12217",
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                                "url": "https://www.alliancegenome.org/disease/DOID:12217"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0060892",
                        "recommended_name": {
                            "id": "DOID:0060892",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0060892",
                            "name": "late onset Parkinson's disease",
                            "description": "A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age."
                        },
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                            {
                                "id": "DOID:0060892",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0060892",
                                "name": "late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PARK",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, age of onset, modifier, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "autosomal dominant late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:168600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/168600",
                                "name": "Parkinson disease",
                                "description": "Parkinson disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0060892",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0060892"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0060892",
                        "recommended_name": {
                            "id": "DOID:0060892",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0060892",
                            "name": "late onset Parkinson's disease",
                            "description": "A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0060892",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0060892",
                                "name": "late onset Parkinson disease",
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                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "LOPD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PARK",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, age of onset, modifier, Multifactorial",
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                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
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                            {
                                "id": "MONDO:0008199",
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                                "id": "MONDO:0008199",
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                                "id": "MONDO:0008199",
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                            {
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                            {
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                            },
                            {
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                            {
                                "id": "MONDO:0007488",
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                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
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                                "description": ""
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                            {
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                                "description": ""
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                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007488",
                                "name": "diffuse Lewy body disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007488",
                                "resource": "MONDO",
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                                "description": ""
                            },
                            {
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                                "resource": "MIM",
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                        ]
                    },
                    {
                        "disease_id": "DOID:0060892",
                        "recommended_name": {
                            "id": "DOID:0060892",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:0060892",
                            "name": "late onset Parkinson's disease",
                            "description": "A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age."
                        },
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                            {
                                "id": "DOID:0060892",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:0060892",
                                "name": "late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "LOPD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PARK",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, age of onset, modifier, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
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                            "url": "http://disease-ontology.org/term/DOID:14330",
                            "name": "Parkinson's disease",
                            "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions."
                        },
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                            {
                                "id": "DOID:14330",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:14330",
                                "name": "Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:14330",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:14330",
                                "name": "paralysis agitans",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "LOPD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PARK",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, age of onset, modifier, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset",
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                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "autosomal dominant late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
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                                "description": ""
                            },
                            {
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                                "name": "late onset Parkinson disease",
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                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:168600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/168600",
                                "name": "Parkinson disease",
                                "description": "Parkinson disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "14330",
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                            },
                            {
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                                "url": "https://www.alliancegenome.org/disease/DOID:14330"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:14330",
                        "recommended_name": {
                            "id": "DOID:14330",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:14330",
                            "name": "Parkinson's disease",
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                            },
                            {
                                "id": "DOID:14330",
                                "resource": "Disease Ontology",
                                "url": "http://disease-ontology.org/term/DOID:14330",
                                "name": "paralysis agitans",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": "A Parkinson disease that begins after around the age of 50."
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "LOPD",
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                            },
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                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0008199",
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                                "name": "PD",
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                            },
                            {
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                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, late-onset, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "Parkinson disease, susceptibility to, Multifactorial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "autosomal dominant late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "hereditary late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late onset Parkinson's disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008199",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008199",
                                "name": "late-onset Parkinson disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:168600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/168600",
                                "name": "Parkinson disease",
                                "description": "Parkinson disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
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                                "id": "14330",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14330"
                            },
                            {
                                "id": "14330",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14330"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            }
        ]
    }
}
