{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010794", 
            "name": "neuropathy, ataxia, and retinitis pigmentosa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010794", 
            "name": "neuropathy-ataxia-retinitis pigmentosa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010794", 
            "name": "neuropathy ataxia retinitis pigmentosa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010794", 
            "name": "NARP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010794", 
            "name": "neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111273", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111273", 
            "name": "Neuropathy-ataxia-retinitis pigmentosa syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111273", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111273", 
            "name": "neuropathy, ataxia and retinitis pigmentosa"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111273", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111273", 
            "name": "Neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/551500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:551500", 
            "name": "Neuropathy, ataxia, and retinitis pigmentosa"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111273", 
        "description": "A mitochondrial metabolism disease characterized by developmental delay, retinitis pigmentosa, dementia, seizures, ataxia, proximal neurogenic muscle weakness, and sensory neuropathy that has_material_basis_in heteroplasmic mutation in the mitochondrial gene MTATP6.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111273", 
        "name": "NARP syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/551500", 
            "id": "551500", 
            "database": "MIM"
        }
    ]
}