{
    "disease_id": "DOID:0111745", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "spinocerebellar ataxia 43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "autosomal dominant cerebellar ataxia caused by mutation in MME"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "spinocerebellar ataxia 43; SCA43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "SCA43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "spinocerebellar ataxia type 43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014867", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014867", 
            "name": "MME autosomal dominant cerebellar ataxia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111745", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111745", 
            "name": "SCA43"
        }, 
        {
            "url": "https://www.omim.org/entry/617018", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617018", 
            "name": "Spinocerebellar ataxia 43"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111745", 
        "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111745", 
        "name": "cerebellar ataxia type 43"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617018", 
            "id": "617018", 
            "database": "MIM"
        }
    ]
}