{
    "disease_id": "DOID:0080286",
    "recommended_name": {
        "id": "DOID:0080286",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080286",
        "name": "spinocerebellar ataxia 44",
        "description": "An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the GRM1 gene on chromosome 6q24."
    },
    "synonyms": [
        {
            "id": "MONDO:0033479",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033479",
            "name": "spinocerebellar ataxia 44",
            "description": ""
        },
        {
            "id": "MONDO:0033479",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033479",
            "name": "spinocerebellar ataxia 44",
            "description": ""
        },
        {
            "id": "MONDO:0033479",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033479",
            "name": "SCA44",
            "description": ""
        },
        {
            "id": "MIM:617691",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617691",
            "name": "Spinocerebellar ataxia 44",
            "description": "Spinocerebellar ataxia 44"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080286"
    ],
    "unlinked_id_list": []
}