{
    "disease_id": "DOID:0111170", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "Adsa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "hereditary ataxia caused by mutation in RNF170"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "ataxia, sensory, 1, autosomal dominant; SNAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "RNF170 hereditary ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "SNAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012166", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012166", 
            "name": "ataxia, sensory, 1, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111170", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111170", 
            "name": "ADSA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111170", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111170", 
            "name": "SNAX1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111170", 
        "description": "A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111170", 
        "name": "autosomal dominant sensory ataxia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111170#disease-associations", 
            "id": "0111170", 
            "database": "Alliance of Genome Resources"
        }
    ]
}