{
    "disease_id": "DOID:0110309",
    "recommended_name": {
        "id": "DOID:0110309",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110309",
        "name": "hypertrophic cardiomyopathy 3",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110309",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110309",
            "name": "CMH3",
            "description": ""
        },
        {
            "id": "DOID:0110309",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110309",
            "name": "cardiomyopathy familial hypertrophic 3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "hypertrophic cardiomyopathy 3",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TPM1 gene."
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "cardiomyopathy, familial hypertrophic, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "TPM1 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "cardiomyopathy familial hypertrophic 3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "cardiomyopathy, familial hypertrophic, 3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "cardiomyopathy, familial hypertrophic, 3; CMH3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "hypertrophic cardiomyopathy caused by mutation in TPM1",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "hypertrophic cardiomyopathy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0007267",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007267",
            "name": "CMH3",
            "description": ""
        },
        {
            "id": "MIM:115196",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/115196",
            "name": "Cardiomyopathy, familial hypertrophic 3",
            "description": "Cardiomyopathy, familial hypertrophic 3"
        }
    ]
}