{
    "disease_id": "DOID:0110314", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "cardiomyopathy, familial hypertrophic, 8; CMH8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "CMH8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "hypertrophic cardiomyopathy type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "cardiomyopathy, familial hypertrophic, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "cardiomyopathy hypertrophic mid-left ventricular chamber type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "MYL3 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "hypertrophic cardiomyopathy caused by mutation in MYL3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012111", 
            "name": "cardiomyopathy, familial hypertrophic, type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110314", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110314", 
            "name": "cardiomyopathy, familial hypertrophic, 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110314", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110314", 
            "name": "cardiomyopathy hypertrophic mid-left ventricular chamber type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110314", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110314", 
        "name": "hypertrophic cardiomyopathy 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110314#disease-associations", 
            "id": "0110314", 
            "database": "Alliance of Genome Resources"
        }
    ]
}