{
    "disease_id": "DOID:0111996", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "IMD51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "candidiasis, familial, 5, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "candidiasis, familial, 5; CANDF5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "candidiasis, familial, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "CANDF5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "candidiasis, familial chronic mucocutaneous, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "immunodeficiency 51; IMD51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013500", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013500", 
            "name": "candidiasis, familial, 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111996", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111996", 
            "name": "CANDF5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111996", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111996", 
            "name": "IMD51"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111996", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111996", 
            "name": "familial candidiasis 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111996", 
        "description": "A primary immunodeficiency disease characterized by onset of chronic mucocutaneous candidiasis in the first years of life and lack of cellular responses to stimulation with certain IL17 isoforms that has_material_basis_in homozygous or compound heterozygous mutation in IL17RA on chromosome 22q11.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111996", 
        "name": "immunodeficiency 51"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111996#disease-associations", 
            "id": "0111996", 
            "database": "Alliance of Genome Resources"
        }
    ]
}