{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "COA5 fatal infantile encephalocardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "fatal infantile encephalocardiomyopathy caused by mutation in COA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3; CEMCOX3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014667", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014667", 
            "name": "CEMCOX3"
        }, 
        {
            "url": "https://www.omim.org/entry/616500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616500", 
            "name": "Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080359", 
        "description": "A fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency that has_material_basis_in homozygous mutation in the COA5 gene on chromosome 2q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080359", 
        "name": "fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616500", 
            "id": "616500", 
            "database": "MIM"
        }
    ]
}