{
    "disease_id": "DOID:0080057",
    "recommended_name": {
        "id": "DOID:0080057",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080057",
        "name": "autosomal recessive spinocerebellar ataxia 15",
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the RUBCN gene on chromosome 3q29."
    },
    "synonyms": [
        {
            "id": "DOID:0080057",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080057",
            "name": "SCAR15",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive spinocerebellar ataxia 15",
            "description": "Any autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome in which the cause of the disease is a mutation in the RUBCN gene."
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "SCAR15",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome caused by mutation in RUBCN",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive spinocerebellar ataxia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "spinocerebellar ataxia, autosomal recessive type 15",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "Salih ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to KIAA0226 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014311",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014311",
            "name": "spinocerebellar ataxia, autosomal recessive 15",
            "description": ""
        },
        {
            "id": "MIM:615705",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615705",
            "name": "Spinocerebellar ataxia, autosomal recessive, 15",
            "description": "Spinocerebellar ataxia, autosomal recessive, 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080057"
    ],
    "unlinked_id_list": []
}