{
    "disease_id": "DOID:0090115", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; SCAN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "spinocerebellar ataxia with axonal neuropathy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "spinocerebellar ataxia, autosomal recessive, with axonal neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "SCAN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "spinocerebellar ataxia with axonal neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "spinocerebellar ataxia autosomal recessive with axonal neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011801", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011801", 
            "name": "autosomal recessive spinocerebellar ataxia with axonal neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090115", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090115", 
            "name": "autosomal recessive spinocerebellar ataxia with axonal neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090115", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090115", 
            "name": "SCAN1"
        }, 
        {
            "url": "https://www.omim.org/entry/607250", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607250", 
            "name": "Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090115", 
        "description": "A nervous system disease characterized by autosomal recessive inheritance of spinocerebellar ataxia and peripheral neuropathy that has_material_basis_in homozygosity for a mutation in the TDP1 gene on chromosome 14q32.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090115", 
        "name": "spinocerebellar ataxia type 1 with axonal neuropathy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607250", 
            "id": "607250", 
            "database": "MIM"
        }
    ]
}