{
    "disease_id": "DOID:0111612",
    "recommended_name": {
        "id": "DOID:0111612",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111612",
        "name": "autosomal recessive spinocerebellar ataxia 3",
        "description": "An autosomal recessive cerebellar ataxia characterized by spinocerebellar ataxia with optic and cochlear degeneration that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 6p23-p21."
    },
    "synonyms": [
        {
            "id": "DOID:0111612",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111612",
            "name": "autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111612",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111612",
            "name": "SCABD",
            "description": ""
        },
        {
            "id": "DOID:0111612",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111612",
            "name": "SCAR3",
            "description": ""
        },
        {
            "id": "DOID:0111612",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111612",
            "name": "autosomal recessive spinocerebellar ataxia type 3",
            "description": ""
        },
        {
            "id": "DOID:0111612",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111612",
            "name": "autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "autosomal recessive cerebellar ataxia-blindness-deafness syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "spinocerebellar ataxia with blindness and deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "spinocerebellar ataxia, autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "SCABD",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "spinocerebellar ataxia autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "autosomal recessive cerebellar ataxia - blindness - deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "autosomal recessive spinocerebellar ataxia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "SCAR3",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "spinocerebellar ataxia, autosomal recessive 3; SCAR3",
            "description": ""
        },
        {
            "id": "MONDO:0010061",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010061",
            "name": "autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome",
            "description": ""
        }
    ]
}