{
    "disease_id": "DOID:0060162",
    "recommended_name": {
        "id": "DOID:0060162",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060162",
        "name": "dentatorubral-pallidoluysian atrophy",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060162",
            "name": "DRPLA",
            "description": ""
        },
        {
            "id": "DOID:0060162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060162",
            "name": "Haw River Syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060162",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060162",
            "name": "Naito-Oyanagi disease",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "dentatorubral-pallidoluysian atrophy",
            "description": "Dentatorubral pallidoluysian atrophy (DRPLA) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by involuntary movements, ataxia, epilepsy, mental disorders, cognitive decline and prominent anticipation."
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "DRPLA",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "Dentatorubropallidoluysian atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "Naito-Oyanagi disease",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "dentatorubral-pallidoluysian atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "haw River syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "NOD",
            "description": ""
        },
        {
            "id": "MONDO:0007435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007435",
            "name": "Naito Oyanagi disease",
            "description": ""
        },
        {
            "id": "MIM:125370",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/125370",
            "name": "Dentatorubral-pallidoluysian atrophy",
            "description": "Dentatorubral-pallidoluysian atrophy"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060162"
    ],
    "unlinked_id_list": []
}