{
    "disease_id": "DOID:0111170",
    "recommended_name": {
        "id": "DOID:0111170",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111170",
        "name": "autosomal dominant sensory ataxia 1",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111170",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111170",
            "name": "ADSA",
            "description": ""
        },
        {
            "id": "DOID:0111170",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111170",
            "name": "SNAX1",
            "description": ""
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "autosomal dominant sensory ataxia 1",
            "description": "Any hereditary ataxia in which the cause of the disease is a mutation in the RNF170 gene."
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "ADSA",
            "description": ""
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "RNF170 hereditary ataxia",
            "description": ""
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "SNAX1",
            "description": ""
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "hereditary ataxia caused by mutation in RNF170",
            "description": ""
        },
        {
            "id": "MONDO:0012166",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012166",
            "name": "ataxia, sensory, 1, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:608984",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608984",
            "name": "Ataxia, sensory, 1, autosomal dominant",
            "description": "Ataxia, sensory, 1, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111170"
    ],
    "unlinked_id_list": []
}