{
    "disease_id": "DOID:0110314",
    "recommended_name": {
        "id": "DOID:0110314",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110314",
        "name": "hypertrophic cardiomyopathy 8",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110314",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110314",
            "name": "cardiomyopathy, familial hypertrophic, 8",
            "description": ""
        },
        {
            "id": "DOID:0110314",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110314",
            "name": "cardiomyopathy hypertrophic mid-left ventricular chamber type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "hypertrophic cardiomyopathy 8",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene."
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "MYL3 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "cardiomyopathy hypertrophic mid-left ventricular chamber type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "cardiomyopathy, familial hypertrophic, 8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "cardiomyopathy, familial hypertrophic, type 8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "cardiomyopathy, hypertrophic, 8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "hypertrophic cardiomyopathy 8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYL3",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "hypertrophic cardiomyopathy type 8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "CMH8",
            "description": ""
        },
        {
            "id": "MONDO:0012111",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012111",
            "name": "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1",
            "description": ""
        },
        {
            "id": "MIM:608751",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608751",
            "name": "Cardiomyopathy, familial hypertrophic, 8",
            "description": "Cardiomyopathy, familial hypertrophic, 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110314"
    ],
    "unlinked_id_list": []
}