{
    "disease_id": "DOID:0110308",
    "recommended_name": {
        "id": "DOID:0110308",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110308",
        "name": "hypertrophic cardiomyopathy 2",
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2)."
    },
    "synonyms": [
        {
            "id": "DOID:0110308",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110308",
            "name": "CMH2",
            "description": ""
        },
        {
            "id": "DOID:0110308",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110308",
            "name": "cardiomyopathy familial hypertrophic 2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "hypertrophic cardiomyopathy 2",
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene."
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "cardiomyopathy, familial hypertrophic, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "TNNT2 hypertrophic cardiomyopathy",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "cardiomyopathy familial hypertrophic 2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "hypertrophic cardiomyopathy caused by mutation in TNNT2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "cardiomyopathy, familial hypertrophic, 2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "cardiomyopathy, familial hypertrophic, 2; CMH2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "CMH2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "familial hypertrophic cardiomyopathy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007266",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007266",
            "name": "hypertrophic cardiomyopathy type 2",
            "description": ""
        },
        {
            "id": "MIM:115195",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/115195",
            "name": "Cardiomyopathy, familial hypertrophic 2",
            "description": "Cardiomyopathy, familial hypertrophic 2"
        }
    ]
}