{
    "disease_id": "DOID:0050984",
    "recommended_name": {
        "id": "DOID:0050984",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050984",
        "name": "spinocerebellar ataxia 37",
        "description": "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0014410",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014410",
            "name": "spinocerebellar ataxia type 37",
            "description": "Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1), characterized by a cerebellar syndrome along with altered vertical eye movements."
        },
        {
            "id": "MONDO:0014410",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014410",
            "name": "SCA37",
            "description": ""
        },
        {
            "id": "MONDO:0014410",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014410",
            "name": "spinocerebellar ataxia with altered vertical eye movements",
            "description": ""
        },
        {
            "id": "MONDO:0014410",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014410",
            "name": "spinocerebellar ataxia 37",
            "description": ""
        },
        {
            "id": "MIM:615945",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615945",
            "name": "Spinocerebellar ataxia 37",
            "description": "Spinocerebellar ataxia 37"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050984"
    ],
    "unlinked_id_list": []
}