{
    "disease_id": "DOID:0110316",
    "recommended_name": {
        "id": "DOID:0110316",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110316",
        "name": "hypertrophic cardiomyopathy 10",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0110316",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110316",
            "name": "CMH10",
            "description": ""
        },
        {
            "id": "DOID:0110316",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110316",
            "name": "cardiomyopathy, familial hypertrophic, 10",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "hypertrophic cardiomyopathy 10",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene."
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "cardiomyopathy, familial hypertrophic, type 10",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "cardiomyopathy, familial hypertrophic, 10",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "cardiomyopathy, familial hypertrophic, 10; CMH10",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "CMH10",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "MYL2 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYL2",
            "description": ""
        },
        {
            "id": "MONDO:0012112",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012112",
            "name": "hypertrophic cardiomyopathy type 10",
            "description": ""
        },
        {
            "id": "MIM:608758",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608758",
            "name": "Cardiomyopathy, familial hypertrophic 10",
            "description": "Cardiomyopathy, familial hypertrophic 10"
        }
    ]
}