{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "mitochondrial DNA depletion syndrome 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "cardiomyopathy and cataract"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "cardiomyopathic mitochondrial DNA depletion syndrome 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "cataract and cardiomyopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008922", 
            "name": "mitochondrial DNA depletion syndrome 10 (Cardiomyopathic type)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080132", 
            "name": "mitochondrial DNA depletion syndrome 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080132", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080132", 
            "name": "mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)"
        }, 
        {
            "url": "https://www.omim.org/entry/212350", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:212350", 
            "name": "Mitochondrial DNA depletion syndrome 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080132", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by congenital cataracts, hypertrophic cardiomyopathy, skeletal myopathy, exercise intolerance, and lactic acidosis, but normal mental development, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the acylglycerol kinase gene on chromosome 7q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080132", 
        "name": "Sengers syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/212350", 
            "id": "212350", 
            "database": "MIM"
        }
    ]
}