{
    "disease_id": "DOID:0090060",
    "recommended_name": {
        "id": "DOID:0090060",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090060",
        "name": "Wolcott-Rallison syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "Wolcott-Rallison syndrome",
            "description": "Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure."
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "WRS",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "Wolcott-Rallison syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "early-onset diabetes mellitus with multiple epiphyseal dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "IDDM-MED syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "MED-IDDM syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "Wolcott Rallison syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009192",
            "name": "epiphyseal dysplasia multiple with early-onset diabetes mellitus",
            "description": ""
        },
        {
            "id": "MIM:226980",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/226980",
            "name": "Wolcott-Rallison syndrome",
            "description": "Wolcott-Rallison syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090060"
    ],
    "unlinked_id_list": []
}