{
    "disease_id": "DOID:0080978",
    "recommended_name": {
        "id": "DOID:0080978",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080978",
        "name": "arthrogryposis multiplex congenita-1",
        "description": "An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0060486",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060486",
            "name": "arthrogryposis multiplex congenita 1, neurogenic, with myelin defect",
            "description": ""
        },
        {
            "id": "MONDO:0060486",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060486",
            "name": "arthrogryposis multiplex congenita, neurogenic, with myelin defect",
            "description": ""
        },
        {
            "id": "MONDO:0060486",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060486",
            "name": "AMCNMY",
            "description": ""
        },
        {
            "id": "MIM:617468",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617468",
            "name": "Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect",
            "description": "Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect"
        }
    ]
}