{
    "disease_id": "DOID:0090060", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "WRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "early-onset diabetes mellitus with multiple epiphyseal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "epiphyseal dysplasia multiple with early-onset diabetes mellitus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "Iddm-Med syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "MED-IDDM syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "epiphyseal dysplasia, multiple, with early-onset diabetes mellitus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009192", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009192", 
            "name": "Wolcott Rallison syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090060", 
        "description": "A syndrome that is characterized by permanent neonatal diabetes mellitus with multiple epiphyseal dysplasia, osteoporosis, growth retardation and frequently hepatic and renal dysfunction that has_material_basis_in homozygous mutation in the eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3) gene on chromosome 2p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090060", 
        "name": "Wolcott-Rallison syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090060#disease-associations", 
            "id": "0090060", 
            "database": "Alliance of Genome Resources"
        }
    ]
}