{
    "disease_id": "DOID:0110316", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "cardiomyopathy, familial hypertrophic, type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "cardiomyopathy, familial hypertrophic, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "cardiomyopathy, familial hypertrophic, 10; CMH10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "CMH10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "MYL2 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "hypertrophic cardiomyopathy caused by mutation in MYL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012112", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012112", 
            "name": "hypertrophic cardiomyopathy type 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110316", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110316", 
            "name": "CMH10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110316", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110316", 
            "name": "cardiomyopathy, familial hypertrophic, 10"
        }, 
        {
            "url": "https://www.omim.org/entry/608758", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608758", 
            "name": "Cardiomyopathy, familial hypertrophic 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110316", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110316", 
        "name": "hypertrophic cardiomyopathy 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608758", 
            "id": "608758", 
            "database": "MIM"
        }
    ]
}