{
    "disease_id": "DOID:0060557", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014084", 
            "name": "AOA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014084", 
            "name": "ataxia-oculomotor apraxia-3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014084", 
            "name": "ataxia-oculomotor apraxia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014084", 
            "name": "ataxia-oculomotor apraxia 3; AOA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014084", 
            "name": "ataxia-oculomotor apraxia 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060557", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060557", 
            "name": "ataxia-oculomotor apraxia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060557", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by poor coordination and balance (ataxia) that worsen over time and that has_material_basis_in  homozygous mutation in the PIK3R5 gene on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060557", 
        "name": "ataxia with oculomotor apraxia type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060557#disease-associations", 
            "id": "0060557", 
            "database": "Alliance of Genome Resources"
        }
    ]
}