{
    "disease_id": "DOID:0070412",
    "recommended_name": {
        "id": "DOID:0070412",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070412",
        "name": "autosomal recessive spinocerebellar ataxia 31",
        "description": "An autosomal recessive cerebellar ataxia characterized by global developmental delay with hypotonia and variably impaired intellectual and language development that has_material_basis_in homozygous or compound heterozygous mutation in the ATG7 gene on chromosome 3p25."
    },
    "synonyms": [
        {
            "id": "DOID:0070412",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070412",
            "name": "SCAR31",
            "description": ""
        },
        {
            "id": "MONDO:0030323",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030323",
            "name": "spinocerebellar ataxia, autosomal recessive 31",
            "description": ""
        },
        {
            "id": "MONDO:0030323",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030323",
            "name": "SCAR31",
            "description": ""
        },
        {
            "id": "MONDO:0030323",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030323",
            "name": "spinocerebellar ataxia, autosomal recessive 31",
            "description": ""
        },
        {
            "id": "MIM:619422",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619422",
            "name": "Spinocerebellar ataxia, autosomal recessive, 31",
            "description": "Spinocerebellar ataxia, autosomal recessive, 31"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070412"
    ],
    "unlinked_id_list": []
}