{
    "disease_id": "DOID:0110308", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "cardiomyopathy, familial hypertrophic, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "TNNT2 hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "cardiomyopathy familial hypertrophic 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "hypertrophic cardiomyopathy caused by mutation in TNNT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "cardiomyopathy, familial hypertrophic, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "cardiomyopathy, familial hypertrophic, 2; CMH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "CMH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "familial hypertrophic cardiomyopathy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007266", 
            "name": "hypertrophic cardiomyopathy type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110308", 
            "name": "CMH2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110308", 
            "name": "cardiomyopathy familial hypertrophic 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110308", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the cardiac troponin-T2 gene (TNNT2).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110308", 
        "name": "hypertrophic cardiomyopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110308#disease-associations", 
            "id": "0110308", 
            "database": "Alliance of Genome Resources"
        }
    ]
}