{
    "disease_id": "DOID:0080981",
    "recommended_name": {
        "id": "DOID:0080981",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080981",
        "name": "arthrogryposis multiplex congenita-5",
        "description": "An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the TOR1A gene on chromosome 9q34."
    },
    "synonyms": [
        {
            "id": "MONDO:0100218",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100218",
            "name": "arthrogryposis multiplex congenita 5",
            "description": ""
        },
        {
            "id": "MONDO:0100218",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100218",
            "name": "AMC5",
            "description": ""
        },
        {
            "id": "MONDO:0100218",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100218",
            "name": "ARTHROGRYPOSIS MULTIPLEX CONGENITA 5",
            "description": ""
        },
        {
            "id": "MIM:618947",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618947",
            "name": "Arthrogryposis multiplex congenita 5",
            "description": "Arthrogryposis multiplex congenita 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080981"
    ],
    "unlinked_id_list": []
}