{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "Tcap hypertrophic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "cardiomyopathy, familial hypertrophic, 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "CMH25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "cardiomyopathy, familial hypertrophic, 25; CMH25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "hypertrophic cardiomyopathy caused by mutation in Tcap"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "cardiomyopathy familial hypertrophic 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "cardiomyopathy, familial hypertrophic, type 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011843", 
            "name": "hypertrophic cardiomyopathy type 25"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110328", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110328", 
            "name": "CMH25"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110328", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110328", 
            "name": "cardiomyopathy familial hypertrophic 25"
        }, 
        {
            "url": "https://www.omim.org/entry/607487", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607487", 
            "name": "Cardiomyopathy, familial hypertrophic 25"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110328", 
        "description": "A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110328", 
        "name": "hypertrophic cardiomyopathy 25"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607487", 
            "id": "607487", 
            "database": "MIM"
        }
    ]
}