{
    "disease_id": "DOID:1440", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "Spinopontine atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "Azorean disease of the nervous system"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "Machado-Joseph disease; MJD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "spinocerebellar ataxia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "spinocerebellar atrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "spinocerebellar atrophy 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "SCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "autosomal dominant striatonigral degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "Azorean neurologic disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "MJD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007182", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007182", 
            "name": "Machado disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1440", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1440", 
            "name": "Azorean disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1440", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1440", 
            "name": "MJD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1440", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1440", 
            "name": "SCA3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1440", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1440", 
            "name": "spinocerebellar ataxia 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1440", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1440", 
            "name": "spinocerebellar ataxia type 3"
        }, 
        {
            "url": "https://www.omim.org/entry/109150", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:109150", 
            "name": "Spinocerebellar ataxia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1440", 
        "description": "An autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has_material_basis_in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1440", 
        "name": "Machado-Joseph disease"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/109150", 
            "id": "109150", 
            "database": "MIM"
        }
    ]
}