{
    "disease_id": "DOID:0110307",
    "recommended_name": {
        "id": "DOID:0110307",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110307",
        "name": "hypertrophic cardiomyopathy 1",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12."
    },
    "synonyms": [
        {
            "id": "DOID:0110307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110307",
            "name": "CMH1",
            "description": ""
        },
        {
            "id": "DOID:0110307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110307",
            "name": "cardiomyopathy, familial hypertrophic 1",
            "description": ""
        },
        {
            "id": "DOID:0110307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110307",
            "name": "hypertrophic cardiomyopathy 19",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy 1",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene."
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "asymmetric septal Hypertrophy",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "MYH7 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "Cmh",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic subaortic stenosis, idiopathic",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "CMH1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy caused by mutation in MYH7",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "hypertrophic cardiomyopathy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "ventricular Hypertrophy, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0008647",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008647",
            "name": "cardiomyopathy, familial hypertrophic, 1; CMH1",
            "description": ""
        },
        {
            "id": "MIM:192600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/192600",
            "name": "Cardiomyopathy, familial hypertrophic",
            "description": "Cardiomyopathy, familial hypertrophic"
        }
    ]
}