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