{
    "disease_id": "DOID:0050941", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "spastic ataxia 2, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "spastic ataxia caused by mutation in KIF1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "KIF1C spastic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "SPG58"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "spastic ataxia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "autosomal recessive spastic paraplegia type 58"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "SPAX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "autosomal recessive spastic ataxia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012651", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012651", 
            "name": "spastic ataxia 2, autosomal recessive; SPAX2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050941", 
        "description": "A spastic ataxia that is characterized by cerebellar ataxia, spasticity and peripheral neuropathy in the first two decades of life, has_material_basis_in homozygous mutation in the KIF1C gene on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050941", 
        "name": "spastic ataxia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050941#disease-associations", 
            "id": "0050941", 
            "database": "Alliance of Genome Resources"
        }
    ]
}