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                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant cervix tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant cervix tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant cervix uteri neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant cervix uteri tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant cervix uteri tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of the cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of the cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of the uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant neoplasm of uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of the cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of the cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of the uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumor of uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of the cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of the cervix uteri",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of the uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant tumour of uterine cervix",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant uterine cervix neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant uterine cervix tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "malignant uterine cervix tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0002974",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0002974",
                                "name": "uterine cervix cancer",
                                "description": ""
                            },
                            {
                                "id": "MIM:603956",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/603956",
                                "name": "Cervical cancer",
                                "description": "Cervical cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "4362",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4362"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111243",
                        "recommended_name": {
                            "id": "DOID:0111243",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111243",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111243",
                                "name": "ACMICD",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111243",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111243",
                                "name": "acromicric skeletal dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric dysplasia",
                                "description": "A rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands."
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "ACMICD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric skeletal dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MIM:102370",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/102370",
                                "name": "Acromicric dysplasia",
                                "description": "Acromicric dysplasia"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "102370",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/102370"
                            },
                            {
                                "id": "0111243",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111150",
                        "recommended_name": {
                            "id": "DOID:0111150",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111150",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111150",
                                "name": "ECTOL1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis 1, isolated, autosomal dominant",
                                "description": "Any isolated ectopia lentis in which the cause of the disease is a mutation in the FBN1 gene."
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ECTOL1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "FBN1 isolated ectopia lentis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis 1, isolated, autosomal dominant",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis, familial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "isolated ectopia lentis caused by mutation in FBN1",
                                "description": ""
                            },
                            {
                                "id": "MIM:129600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/129600",
                                "name": "Ectopia lentis 1, isolated, autosomal dominant",
                                "description": "Ectopia lentis 1, isolated, autosomal dominant"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "129600",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/129600"
                            },
                            {
                                "id": "0111150",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111726",
                        "recommended_name": {
                            "id": "DOID:0111726",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111726",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111726",
                                "name": "GPHYSD2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "geleophysic dysplasia 2",
                                "description": "Any geleophysic dysplasia in which the cause of the disease is a mutation in the FBN1 gene."
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "FBN1 geleophysic dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "geleophysic dysplasia caused by mutation in FBN1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "GPHYSD2",
                                "description": ""
                            },
                            {
                                "id": "MIM:614185",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614185",
                                "name": "Geleophysic dysplasia 2",
                                "description": "Geleophysic dysplasia 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614185",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614185"
                            },
                            {
                                "id": "0111726",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:14323",
                        "recommended_name": {
                            "id": "DOID:14323",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:14323",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:14323",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": "A disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, walls of blood vessels, and heart valves. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). It is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Marfan syndrome is inherited in an autosomal dominant pattern. At least 25% of cases are due to a new (de novo) mutation. Treatment is based on the signs and symptoms in each person."
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MIM:154700",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/154700",
                                "name": "Marfan syndrome",
                                "description": "Marfan syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "14323",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14323"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111561",
                        "recommended_name": {
                            "id": "DOID:0111561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111561",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": "A rare syndrome characterized by hard, thick skin, usually on the entire body. The thickening of the skin can limit joint mobility and causes joints to be stuck in a bent position (flexion contractures). The onset of signs and symptoms can range from presenting at birth through childhood. Other signs and symptoms may include excessive hair growth (hypertrichosis), loss of body fat (lipodystrophy), scoliosis, muscle weakness, slow growth, and short stature. Weakness or paralysis of the eye muscles have also been reported. Stiff skin syndrome is caused by mutations (changes) in the FBN1 gene and is inherited in an autosomal dominant manner. Diagnosis is based on a clinical evaluation that is consistent with stiff skin syndrome, and the diagnosis can be confirmed with genetic testing. Treatment is based on the symptoms of each individual and may include physical therapy."
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MIM:184900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/184900",
                                "name": "Stiff skin syndrome",
                                "description": "Stiff skin syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "184900",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/184900"
                            },
                            {
                                "id": "0111561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0061274",
                        "recommended_name": {
                            "id": "DOID:0061274",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0061274",
                            "name": "Weill-Marchesani syndrome 2",
                            "description": "A Weill-Marchesani syndrome that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome 2, dominant",
                                "description": "A Weill-Marchesani syndrome characterized by progressive joint stiffness, glaucoma, short stature and lens dislocation. It has been described in three members of a family (the grandfather, his daughter and grandson). It is likely to be transmitted as an autosomal dominant trait. The acronym GEMSS (Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature) was proposed as a name for the syndrome. This syndrome shows similarities to Moore-Federman syndrome."
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "mesodermal Dysmorphodystrophy, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "spherophakia-brachymorphia syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/11826022"
                    },
                    {
                        "id": "12446365",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/12446365"
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                    {
                        "id": "15054843",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/15054843"
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                    {
                        "id": "17701892",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/17701892"
                    },
                    {
                        "id": "20375004",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20375004"
                    },
                    {
                        "id": "7802039",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/7802039"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-gain"
                ],
                "start_pos": 240,
                "end_pos": 240,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 1 filters: n-glyco-sequon-gain (NIR->NIC).",
                "chr_id": "15",
                "chr_pos": "48537629",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R240",
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                    {
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                            {
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                            {
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                            {
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                            {
                                "id": "MONDO:0002974",
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                            {
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                            {
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                            {
                                "id": "MONDO:0002974",
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                            {
                                "id": "MONDO:0002974",
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                            },
                            {
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
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                            },
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                            },
                            {
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                                "name": "Ectopia lentis 1, isolated, autosomal dominant",
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                            {
                                "id": "0111150",
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                        ]
                    },
                    {
                        "disease_id": "DOID:0111726",
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                            "resource": "Disease Ontology",
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                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
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                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "FBN1 geleophysic dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "geleophysic dysplasia caused by mutation in FBN1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "GPHYSD2",
                                "description": ""
                            },
                            {
                                "id": "MIM:614185",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614185",
                                "name": "Geleophysic dysplasia 2",
                                "description": "Geleophysic dysplasia 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614185",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614185"
                            },
                            {
                                "id": "0111726",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:14323",
                        "recommended_name": {
                            "id": "DOID:14323",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:14323",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:14323",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": "A disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, walls of blood vessels, and heart valves. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). It is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Marfan syndrome is inherited in an autosomal dominant pattern. At least 25% of cases are due to a new (de novo) mutation. Treatment is based on the signs and symptoms in each person."
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MIM:154700",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/154700",
                                "name": "Marfan syndrome",
                                "description": "Marfan syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "14323",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14323"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111561",
                        "recommended_name": {
                            "id": "DOID:0111561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111561",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": "A rare syndrome characterized by hard, thick skin, usually on the entire body. The thickening of the skin can limit joint mobility and causes joints to be stuck in a bent position (flexion contractures). The onset of signs and symptoms can range from presenting at birth through childhood. Other signs and symptoms may include excessive hair growth (hypertrichosis), loss of body fat (lipodystrophy), scoliosis, muscle weakness, slow growth, and short stature. Weakness or paralysis of the eye muscles have also been reported. Stiff skin syndrome is caused by mutations (changes) in the FBN1 gene and is inherited in an autosomal dominant manner. Diagnosis is based on a clinical evaluation that is consistent with stiff skin syndrome, and the diagnosis can be confirmed with genetic testing. Treatment is based on the symptoms of each individual and may include physical therapy."
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MIM:184900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/184900",
                                "name": "Stiff skin syndrome",
                                "description": "Stiff skin syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "184900",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/184900"
                            },
                            {
                                "id": "0111561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0061274",
                        "recommended_name": {
                            "id": "DOID:0061274",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0061274",
                            "name": "Weill-Marchesani syndrome 2",
                            "description": "A Weill-Marchesani syndrome that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome 2, dominant",
                                "description": "A Weill-Marchesani syndrome characterized by progressive joint stiffness, glaucoma, short stature and lens dislocation. It has been described in three members of a family (the grandfather, his daughter and grandson). It is likely to be transmitted as an autosomal dominant trait. The acronym GEMSS (Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature) was proposed as a name for the syndrome. This syndrome shows similarities to Moore-Federman syndrome."
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "mesodermal Dysmorphodystrophy, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "spherophakia-brachymorphia syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "GEMSS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "GEMSS syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "WMS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome, autosomal dominant",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome",
                                "description": ""
                            },
                            {
                                "id": "MIM:608328",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/608328",
                                "name": "Weill-Marchesani syndrome 2",
                                "description": "Weill-Marchesani syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "608328",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/608328"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
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        ],
        "record_id": "pubmed.7802039",
        "abstract": "",
        "glycosylation": [],
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        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
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                    },
                    {
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                    },
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                        "field": "o_linked_glycans",
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                ],
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            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
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                ],
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            {
                "table_id": "glycosylation_reported",
                "table_stats": [
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                    {
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                    {
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                    {
                        "field": "n_linked_glycan_sites",
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                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
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                        "field": "total",
                        "count": 0
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                    {
                        "field": "total_sites",
                        "count": 0
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                        "count": 0
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                    {
                        "field": "o_linked_sites",
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                    },
                    {
                        "field": "n_linked_glycan_sites",
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                    {
                        "field": "o_linked_glycan_sites",
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                    {
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
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                    {
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_automatic_literature_mining",
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                        "count": 0
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                    {
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                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "A novel mutation in the fibrillin gene (FBN1) in familial arachnodactyly.",
        "journal": "Molecular and cellular probes",
        "date": "1994",
        "authors": "Hayward C, Porteous ME, Brock DJ",
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            "type": "PubMed",
            "id": "7870075",
            "url": "https://pubmed.ncbi.nlm.nih.gov/7870075"
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                "protein_name": "Fibrillin-1",
                "gene_name": "FBN1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
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                        "id": "P35555",
                        "url": "https://www.uniprot.org/uniprotkb/P35555"
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                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.7870075",
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        "section_stats": [
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            {
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            {
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        ]
    },
    {
        "title": "Identification of a novel nonsense mutation in the fibrillin gene (FBN1) using nonisotopic techniques.",
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        "date": "1994",
        "authors": "Hayward C, Porteous ME, Brock DJ",
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        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P35555-1",
                "protein_name": "Fibrillin-1",
                "gene_name": "FBN1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P35555",
                        "url": "https://www.uniprot.org/uniprotkb/P35555"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "P35555",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P35555"
                    },
                    {
                        "id": "rs137854467",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137854467"
                    },
                    {
                        "id": "rs137854467",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs137854467"
                    },
                    {
                        "id": "8040326",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/8040326"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-gain"
                ],
                "start_pos": 122,
                "end_pos": 122,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 1 filters: n-glyco-sequon-gain (NIR->NIC).",
                "chr_id": "15",
                "chr_pos": "48600217",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R122",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
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                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111243",
                        "recommended_name": {
                            "id": "DOID:0111243",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111243",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111243",
                                "name": "ACMICD",
                                "description": ""
                            },
                            {
                                "id": "DOID:0111243",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111243",
                                "name": "acromicric skeletal dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric dysplasia",
                                "description": "A rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands."
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "ACMICD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007055",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007055",
                                "name": "Acromicric skeletal dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MIM:102370",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/102370",
                                "name": "Acromicric dysplasia",
                                "description": "Acromicric dysplasia"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "102370",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/102370"
                            },
                            {
                                "id": "0111243",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111150",
                        "recommended_name": {
                            "id": "DOID:0111150",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111150",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111150",
                                "name": "ECTOL1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis 1, isolated, autosomal dominant",
                                "description": "Any isolated ectopia lentis in which the cause of the disease is a mutation in the FBN1 gene."
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ECTOL1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "FBN1 isolated ectopia lentis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis 1, isolated, autosomal dominant",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "ectopia lentis, familial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007514",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007514",
                                "name": "isolated ectopia lentis caused by mutation in FBN1",
                                "description": ""
                            },
                            {
                                "id": "MIM:129600",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/129600",
                                "name": "Ectopia lentis 1, isolated, autosomal dominant",
                                "description": "Ectopia lentis 1, isolated, autosomal dominant"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "129600",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/129600"
                            },
                            {
                                "id": "0111150",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111726",
                        "recommended_name": {
                            "id": "DOID:0111726",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111726",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111726",
                                "name": "GPHYSD2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "geleophysic dysplasia 2",
                                "description": "Any geleophysic dysplasia in which the cause of the disease is a mutation in the FBN1 gene."
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "FBN1 geleophysic dysplasia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "Geleophysic dysplasia type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "geleophysic dysplasia caused by mutation in FBN1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013612",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013612",
                                "name": "GPHYSD2",
                                "description": ""
                            },
                            {
                                "id": "MIM:614185",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614185",
                                "name": "Geleophysic dysplasia 2",
                                "description": "Geleophysic dysplasia 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614185",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614185"
                            },
                            {
                                "id": "0111726",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:14323",
                        "recommended_name": {
                            "id": "DOID:14323",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:14323",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:14323",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": "A disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, walls of blood vessels, and heart valves. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). It is caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. Marfan syndrome is inherited in an autosomal dominant pattern. At least 25% of cases are due to a new (de novo) mutation. Treatment is based on the signs and symptoms in each person."
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "MFS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan syndrome, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007947",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007947",
                                "name": "Marfan's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MIM:154700",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/154700",
                                "name": "Marfan syndrome",
                                "description": "Marfan syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "14323",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:14323"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111561",
                        "recommended_name": {
                            "id": "DOID:0111561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111561",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": "A rare syndrome characterized by hard, thick skin, usually on the entire body. The thickening of the skin can limit joint mobility and causes joints to be stuck in a bent position (flexion contractures). The onset of signs and symptoms can range from presenting at birth through childhood. Other signs and symptoms may include excessive hair growth (hypertrichosis), loss of body fat (lipodystrophy), scoliosis, muscle weakness, slow growth, and short stature. Weakness or paralysis of the eye muscles have also been reported. Stiff skin syndrome is caused by mutations (changes) in the FBN1 gene and is inherited in an autosomal dominant manner. Diagnosis is based on a clinical evaluation that is consistent with stiff skin syndrome, and the diagnosis can be confirmed with genetic testing. Treatment is based on the symptoms of each individual and may include physical therapy."
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "stiff skin syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008492",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008492",
                                "name": "SSKS",
                                "description": ""
                            },
                            {
                                "id": "MIM:184900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/184900",
                                "name": "Stiff skin syndrome",
                                "description": "Stiff skin syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "184900",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/184900"
                            },
                            {
                                "id": "0111561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0061274",
                        "recommended_name": {
                            "id": "DOID:0061274",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0061274",
                            "name": "Weill-Marchesani syndrome 2",
                            "description": "A Weill-Marchesani syndrome that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome 2, dominant",
                                "description": "A Weill-Marchesani syndrome characterized by progressive joint stiffness, glaucoma, short stature and lens dislocation. It has been described in three members of a family (the grandfather, his daughter and grandson). It is likely to be transmitted as an autosomal dominant trait. The acronym GEMSS (Glaucoma, Ectopia, Microspherophakia, Stiff joints, Short stature) was proposed as a name for the syndrome. This syndrome shows similarities to Moore-Federman syndrome."
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "mesodermal Dysmorphodystrophy, congenital",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "spherophakia-brachymorphia syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "GEMSS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "GEMSS syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "WMS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "Weill-Marchesani syndrome, autosomal dominant",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012013",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012013",
                                "name": "glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome",
                                "description": ""
                            },
                            {
                                "id": "MIM:608328",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/608328",
                                "name": "Weill-Marchesani syndrome 2",
                                "description": "Weill-Marchesani syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "608328",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/608328"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
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        ],
        "record_id": "pubmed.8040326",
        "abstract": "",
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        "phosphorylation": [],
        "glycation": [],
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                "table_id": "referenced_proteins",
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            {
                "table_id": "phosphorylation",
                "table_stats": [
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                ],
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            {
                "table_id": "glycosylation_reported",
                "table_stats": [
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                    {
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                    {
                        "field": "n_linked_glycan_sites",
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                    {
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                    },
                    {
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                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
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                    {
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                    },
                    {
                        "field": "n_linked_glycan_sites",
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                    {
                        "field": "o_linked_glycan_sites",
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                    {
                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
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                        "count": 0
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
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                        "count": 0
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                    {
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                        "count": 0
                    }
                ],
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        ]
    },
    {
        "title": "A new missense mutation of fibrillin in a patient with Marfan syndrome.",
        "journal": "Journal of medical genetics",
        "date": "1994",
        "authors": "Hewett DR, Lynch JR, Child A, Sykes BC",
        "reference": {
            "type": "PubMed",
            "id": "8071963",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8071963"
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                "tax_name": "Human"
            }
        ],
        "species": [
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                "name": "Homo sapiens",
                "taxid": 9606,
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                        "database": "UniProtKB",
                        "id": "P35555",
                        "url": "https://www.uniprot.org/uniprotkb/P35555"
                    }
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                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.8071963",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
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        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
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                ],
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                ]
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                "table_stats": [
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                        "count": 0
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                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
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                    },
                    {
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                    },
                    {
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                        "count": 0
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                    {
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                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
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                        "count": 0
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                    {
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                    }
                ],
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            {
                "table_id": "glycosylation_reported",
                "table_stats": [
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                        "count": 0
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                        "count": 0
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                    {
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    {
        "title": "Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.",
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        "authors": "Kainulainen K, Karttunen L, Puhakka L, Sakai L, Peltonen L",
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    {
        "title": "Crystal structure of the human Pax-6 paired domain-DNA complex reveals specific roles for the linker region and carboxyl-terminal subdomain in DNA binding.",
        "journal": "Genes Dev.",
        "date": "1999",
        "authors": "Xu H E, Rould M A, Xu W, Epstein J A, Maas R L, Pabo C O",
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            "id": "10346815",
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                "taxid": 9606,
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        "abstract": "",
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