{
    "disease_id": "DOID:0110323", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "cardiomyopathy, familial hypertrophic, 17; CMH17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "cardiomyopathy, familial hypertrophic, type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "hypertrophic cardiomyopathy type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "JPH2 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "cardiomyopathy, familial hypertrophic, 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "cardiomyopathy familial hypertrophic 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "CMH17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013474", 
            "name": "hypertrophic cardiomyopathy caused by mutation in JPH2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110323", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110323", 
            "name": "CMH17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110323", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110323", 
            "name": "cardiomyopathy familial hypertrophic 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110323", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110323", 
        "name": "hypertrophic cardiomyopathy 17"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110323#disease-associations", 
            "id": "0110323", 
            "database": "Alliance of Genome Resources"
        }
    ]
}