{
    "disease_id": "DOID:0050999",
    "recommended_name": {
        "id": "DOID:0050999",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050999",
        "name": "autosomal recessive spinocerebellar ataxia 10",
        "description": "An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050999",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050999",
            "name": "SCAR10",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "autosomal recessive spinocerebellar ataxia 10",
            "description": "Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the ANO10 gene."
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "ANO10 autosomal recessive cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "SCAR10",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "autosomal recessive cerebellar ataxia caused by mutation in ANO10",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "autosomal recessive spinocerebellar ataxia type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "spinocerebellar ataxia, autosomal recessive type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013392",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013392",
            "name": "spinocerebellar ataxia, autosomal recessive 10",
            "description": ""
        },
        {
            "id": "MIM:613728",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613728",
            "name": "Spinocerebellar ataxia, autosomal recessive, 10",
            "description": "Spinocerebellar ataxia, autosomal recessive, 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050999"
    ],
    "unlinked_id_list": []
}