{
    "disease_id": "DOID:0060602", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013681", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013681", 
            "name": "ALPHA-methylacyl-CoA racemase deficiency; AMACRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013681", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013681", 
            "name": "AMACR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013681", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013681", 
            "name": "AMACRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013681", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013681", 
            "name": "AMACR deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060602", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060602", 
            "name": "AMACR deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060602", 
        "description": "A peroxisomal disease that is characterized by retinitis pigmentosa resulting in progressive visual failure, learning difficulties, a peripheral neuropathy, and hypogonadism and that has_material_basis in homozygous mutation in the AMACR gene on chromosome 5p13.2-q11.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060602", 
        "name": "alpha-methylacyl-CoA racemase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060602#disease-associations", 
            "id": "0060602", 
            "database": "Alliance of Genome Resources"
        }
    ]
}