{
    "disease_id": "DOID:0050958", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "ADCA, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "OPCA with macular Degeneration and external ophthalmoplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "SCA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "OPCA 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "olivopontocerebellar atrophy 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "Adca, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "cerebellar syndrome-pigmentary maculopathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "OPCA with retinal Degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "ATXN7 autosomal dominant cerebellar ataxia type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "OPCA III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "ataxia with pigmentary retinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "spinocerebellar ataxia 7; SCA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "spinocerebellar ataxia 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "autosomal dominant cerebellar ataxia, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008120", 
            "name": "OPCA3"
        }, 
        {
            "url": "https://www.omim.org/entry/164500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:164500", 
            "name": "Spinocerebellar ataxia 7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050958", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050958", 
        "name": "spinocerebellar ataxia type 7"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/164500", 
            "id": "164500", 
            "database": "MIM"
        }
    ]
}