{
    "disease_id": "DOID:0080337", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "mitochondrial DNA depletion syndrome 15 (hepatocerebral type);"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "mitochondrial DNA depletion syndrome caused by mutation in TFAM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "MTDPS15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "TFAM mitochondrial DNA depletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "mitochondrial DNA depletion syndrome 15 (hepatocerebral type)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014943", 
            "name": "mitochondrial DNA depletion syndrome 15 (hepatocerebral type); MTDPS15"
        }, 
        {
            "url": "https://www.omim.org/entry/617156", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617156", 
            "name": "Mitochondrial DNA depletion syndrome 15, hepatocerebral type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080337", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by severe intrauterine growth restriction, neonatal-onset hypoglycemia and liver dysfunction, mitochondrial DNA depletion in liver and skeletal muscle, and abnormal mitochondrial morphology observed in skeletal muscle, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the mitochondrial transcription factor A gene on chromosome 10q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080337", 
        "name": "mitochondrial DNA depletion syndrome 15"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617156", 
            "id": "617156", 
            "database": "MIM"
        }
    ]
}