{
    "disease_id": "DOID:0110322",
    "recommended_name": {
        "id": "DOID:0110322",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110322",
        "name": "hypertrophic cardiomyopathy 16",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26."
    },
    "synonyms": [
        {
            "id": "DOID:0110322",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110322",
            "name": "CMH16",
            "description": ""
        },
        {
            "id": "DOID:0110322",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110322",
            "name": "cardiomyopathy familial hypertrophic 16",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "hypertrophic cardiomyopathy 16",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene."
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "CMH16",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "MYOZ2 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "cardiomyopathy, familial hypertrophic, type 16",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "cardiomyopathy, hypertrophic, 16",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYOZ2",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "hypertrophic cardiomyopathy type 16",
            "description": ""
        },
        {
            "id": "MONDO:0013455",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013455",
            "name": "cardiomyopathy, familial hypertrophic, 16",
            "description": ""
        },
        {
            "id": "MIM:613838",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613838",
            "name": "Cardiomyopathy, familial hypertrophic, 16",
            "description": "Cardiomyopathy, familial hypertrophic, 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110322"
    ],
    "unlinked_id_list": []
}