{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "cardiomyopathy, familial hypertrophic, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "TNNI3 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "cardiomyopathy, familial hypertrophic, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "hypertrophic cardiomyopathy caused by mutation in TNNI3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "cardiomyopathy, familial hypertrophic 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "CMH7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "cardiomyopathy, familial hypertrophic, 7; CMH7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013369", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013369", 
            "name": "hypertrophic cardiomyopathy type 7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110313", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110313", 
            "name": "CMH7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110313", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110313", 
            "name": "cardiomyopathy, familial hypertrophic 7"
        }, 
        {
            "url": "https://www.omim.org/entry/613690", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613690", 
            "name": "Cardiomyopathy, familial hypertrophic 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110313", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110313", 
        "name": "hypertrophic cardiomyopathy 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613690", 
            "id": "613690", 
            "database": "MIM"
        }
    ]
}