{
    "disease_id": "DOID:0111753", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010777", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010777", 
            "name": "cardiomyopathy, infantile hypertrophic"
        }, 
        {
            "url": "https://www.omim.org/entry/500006", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:500006", 
            "name": "Cardiomyopathy, infantile hypertrophic"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111753", 
        "description": "A hypertrophic cardiomyopathy characterized by isolated hypertrophic cardiomyopathy and congestive heart failure that has_material_basis_in mutation in the overlapping mitochondrial genes MTATP6 and MTATP8.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111753", 
        "name": "infantile hypertrophic cardiomyopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500006", 
            "id": "500006", 
            "database": "MIM"
        }
    ]
}