{
    "disease_id": "DOID:0080123", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "mitochondrial DNA depletion syndrome type 4b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "mitochondrial neurogastrointestinal encephalopathy syndrome, Polg-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "Mngie, Polg-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "mitochondrial DNA depletion syndrome 4B (MNGIE type); MTDPS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "MTDPS4B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013350", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013350", 
            "name": "mitochondrial DNA depletion syndrome 4B (MNGIE type)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080123", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080123", 
            "name": "mitochondrial neurogastrointestinal encephalopathy syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080123", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by chronic gastrointestinal dysmotility and pseudoobstruction, cachexia, progressive external ophthalmoplegia, axonal sensory ataxic neuropathy, and muscle weakness, and has_material_basis_in autosomal recessive inheritance of compound heterozygous mutation in the mitochondrial DNA polymerase gamma gene on chromosome 15q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080123", 
        "name": "mitochondrial DNA depletion syndrome 4b"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613662", 
            "id": "613662", 
            "database": "MIM"
        }
    ]
}