{
    "disease_id": "DOID:0060162", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "haw River syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "DRPLA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "NOD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "ataxia, chorea, seizures, and dementia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "dentatorubral pallidoluysian atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "Dentatorubropallidoluysian atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "myoclonic epilepsy with choreoathetosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "Naito-Oyanagi disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "Naito Oyanagi disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007435", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007435", 
            "name": "dentatorubral-pallidoluysian atrophy; DRPLA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060162", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060162", 
            "name": "DRPLA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060162", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060162", 
            "name": "Haw River Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060162", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060162", 
            "name": "Naito-Oyanagi disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060162", 
        "description": "An autosomal dominant cerebellar ataxia that has_material_basis_in expansion of  CAG triplet repeats (glutamine) encoding a polyglutamine tract in the atrophin-1 protein.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060162", 
        "name": "dentatorubral-pallidoluysian atrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/125370", 
            "id": "125370", 
            "database": "MIM"
        }
    ]
}