{
    "disease_id": "DOID:0080198", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "histiocytoid cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "Purkinje cell hamartoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "cardiomyopathy, oncocytic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "cardiomyopathy, infantile xanthomatous"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "myocardial hamartoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "infantile cardiomyopathy with histiocytoid change"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "congenital cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "infantile xanthomatous cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "isolated Cardiac lipidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "focal lipid cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "cardiomyopathy, focal Lipid"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "oncocytic cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "Arachnocytosis of the myocardium"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "foamy myocardial transformation of infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010771", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010771", 
            "name": "cardiomyopathy, infantile histiocytoid"
        }, 
        {
            "url": "https://www.omim.org/entry/500000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:500000", 
            "name": "Cardiomyopathy, infantile histiocytoid"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080198", 
        "description": "An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080198", 
        "name": "infantile histiocytoid cardiomyopathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/500000", 
            "id": "500000", 
            "database": "MIM"
        }
    ]
}