{
    "disease_id": "DOID:1926", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:1926", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1926", 
            "name": "Gaucher disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1926", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1926", 
            "name": "acid beta-glucosidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1926", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1926", 
            "name": "glocucerebrosidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1926", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1926", 
            "name": "glucosylceramide beta-glucosidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1926", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1926", 
            "name": "kerasin thesaurismosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1926", 
        "description": "A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1926", 
        "name": "Gaucher's disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1926#disease-associations", 
            "id": "1926", 
            "database": "Alliance of Genome Resources"
        }
    ]
}