{
    "disease_id": "DOID:0111974", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009305", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009305", 
            "name": "granulocytopenia with immunoglobulin abnormality"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111974", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111974", 
            "name": "IMD59"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111974", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111974", 
            "name": "granulocytopenia with immunoglobin abnormality"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111974", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111974", 
            "name": "immunodeficiency 59 and hypoglycemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111974", 
        "description": "A B cell and dendritic cell deficiency characterized by granulocytopenia, B-cell and dentritic cell deficiency, recurrent septic infections of the respiratory tract, skin, and mucous membranes, and stress-induced hypoglycemia that has_material_basis_in homozygous or compound heterozygous mutation in HYOU1 on chromosome 11q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111974", 
        "name": "immunodeficiency 59"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111974#disease-associations", 
            "id": "0111974", 
            "database": "Alliance of Genome Resources"
        }
    ]
}