{
    "disease_id": "DOID:0111613",
    "recommended_name": {
        "id": "DOID:0111613",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111613",
        "name": "autosomal recessive spinocerebellar ataxia 23",
        "description": "An autosomal recessive cerebellar ataxia characterized by epilepsy, intellectual disability, and gait ataxia that has_material_basis_in homozygous or compound heterozygous mutation in TDP2 on chromosome 6p22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111613",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111613",
            "name": "SCAR23",
            "description": ""
        },
        {
            "id": "DOID:0111613",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111613",
            "name": "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "spinocerebellar ataxia, autosomal recessive type 23",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "SCAR23",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "spinocerebellar ataxia autosomal recessive type 23",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "spinocerebellar ataxia, autosomal recessive 23; SCAR23",
            "description": ""
        },
        {
            "id": "MONDO:0014846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014846",
            "name": "spinocerebellar ataxia, autosomal recessive 23",
            "description": ""
        },
        {
            "id": "MIM:616949",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616949",
            "name": "Spinocerebellar ataxia, autosomal recessive, 23",
            "description": "Spinocerebellar ataxia, autosomal recessive, 23"
        }
    ]
}