{
    "disease_id": "DOID:0050772", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "spastic ataxia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "autosomal dominant spastic ataxia caused by mutation in VAMP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "SPAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "autosomal dominant spastic ataxia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "spastic ataxia 1, autosomal dominant; SPAX1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "VAMP1 autosomal dominant spastic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007164", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007164", 
            "name": "spastic ataxia 1, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050772", 
        "description": "A spastic ataxia characterized by early-onset cerebellar ataxia, spasticity, pyramidal syndrome and peripheral neuropathy, has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the VAMP1 gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050772", 
        "name": "spastic ataxia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050772#disease-associations", 
            "id": "0050772", 
            "database": "Alliance of Genome Resources"
        }
    ]
}