{
    "disease_id": "DOID:0110312", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110312", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110312", 
            "name": "cardiomyopathy, familial hypertrophic 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110312", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110312", 
            "name": "CMH6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the PRKAG2 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "hypertrophic cardiomyopathy 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "PRKAG2 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "hypertrophic cardiomyopathy type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "cardiomyopathy, familial hypertrophic, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "cardiomyopathy, familial hypertrophic, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "cardiomyopathy, familial hypertrophic 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "hypertrophic cardiomyopathy caused by mutation in PRKAG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "cardiomyopathy, familial hypertrophic, 6; CMH6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010946", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010946", 
            "name": "CMH6"
        }, 
        {
            "url": "https://www.omim.org/entry/600858", 
            "description": "Cardiomyopathy, familial hypertrophic 6", 
            "resource": "MIM", 
            "id": "MIM:600858", 
            "name": "Cardiomyopathy, familial hypertrophic 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110312", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110312", 
        "name": "hypertrophic cardiomyopathy 6"
    }
}