{
    "disease_id": "DOID:0050999", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "ANO10 autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "spinocerebellar ataxia, autosomal recessive 10; SCAR10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "autosomal recessive spinocerebellar ataxia type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "autosomal recessive cerebellar ataxia caused by mutation in ANO10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "spinocerebellar ataxia, autosomal recessive type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "adult-onset autosomal recessive cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "SCAR10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013392", 
            "name": "spinocerebellar ataxia, autosomal recessive 10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050999", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050999", 
            "name": "SCAR10"
        }, 
        {
            "url": "https://www.omim.org/entry/613728", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613728", 
            "name": "Spinocerebellar ataxia, autosomal recessive, 10"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050999", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050999", 
        "name": "autosomal recessive spinocerebellar ataxia 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613728", 
            "id": "613728", 
            "database": "MIM"
        }
    ]
}