{
    "disease_id": "DOID:0080979",
    "recommended_name": {
        "id": "DOID:0080979",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080979",
        "name": "arthrogryposis multiplex congenita-3",
        "description": "An arthrogryposis multiplex congenita that is characterized by decreased fetal movements, hypotonia, variable skeletal defects, including clubfoot and scoliosis, and delayed motor milestones with difficulty walking and that has_material_basis_in homozygous or compound heterozygous mutation in the SYNE1 gene on chromosome 6q25."
    },
    "synonyms": [
        {
            "id": "MONDO:0032778",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032778",
            "name": "arthrogryposis multiplex congenita 3, myogenic type",
            "description": ""
        },
        {
            "id": "MONDO:0032778",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032778",
            "name": "AMCM",
            "description": ""
        },
        {
            "id": "MONDO:0032778",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032778",
            "name": "arthrogryposis multiplex congenita, myogenic type",
            "description": ""
        },
        {
            "id": "MIM:618484",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618484",
            "name": "Arthrogryposis multiplex congenita 3, myogenic type",
            "description": "Arthrogryposis multiplex congenita 3, myogenic type"
        }
    ]
}