{
    "disease_id": "DOID:0070409",
    "recommended_name": {
        "id": "DOID:0070409",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070409",
        "name": "autosomal recessive spinocerebellar ataxia 28",
        "description": "An autosomal recessive cerebellar ataxia characterized by onset in early childhood of mildly delayed motor development, gait ataxia, incoordination of fine motor movements, and dysarthria that has_material_basis_in homozygous mutation in the THG1L gene on chromosome 5q33."
    },
    "synonyms": [
        {
            "id": "DOID:0070409",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070409",
            "name": "SCAR28",
            "description": ""
        },
        {
            "id": "MONDO:0032923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032923",
            "name": "spinocerebellar ataxia, autosomal recessive 28",
            "description": ""
        },
        {
            "id": "MONDO:0032923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032923",
            "name": "THG1L-related autosomal recessive congenital cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0032923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032923",
            "name": "SCAR28",
            "description": ""
        },
        {
            "id": "MIM:618800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618800",
            "name": "Spinocerebellar ataxia, autosomal recessive, 28",
            "description": "Spinocerebellar ataxia, autosomal recessive, 28"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070409"
    ],
    "unlinked_id_list": []
}