{
    "disease_id": "DOID:0111753",
    "recommended_name": {
        "id": "DOID:0111753",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111753",
        "name": "infantile hypertrophic cardiomyopathy",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0010777",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010777",
            "name": "cardiomyopathy, infantile hypertrophic",
            "description": ""
        },
        {
            "id": "MIM:500006",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/500006",
            "name": "Cardiomyopathy, infantile hypertrophic",
            "description": "Cardiomyopathy, infantile hypertrophic"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111753"
    ],
    "unlinked_id_list": []
}