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