{
    "disease_id": "DOID:0061015",
    "recommended_name": {
        "id": "DOID:0061015",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061015",
        "name": "female-restricted Wieacker-Wolff syndrome",
        "description": "A syndromic X-linked intellectual disability that has_material_basis_in heterozygous mutation in the ZC4H2 gene on chromosome Xq11."
    },
    "synonyms": [
        {
            "id": "DOID:0061015",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061015",
            "name": "WRWFFR",
            "description": ""
        },
        {
            "id": "MONDO:0026762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026762",
            "name": "Wieacker-Wolff syndrome, female-restricted",
            "description": ""
        },
        {
            "id": "MONDO:0026762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026762",
            "name": "Wieacker-Wolff syndrome, female-restricted, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0026762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026762",
            "name": "WRWFFR",
            "description": ""
        },
        {
            "id": "MIM:301041",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301041",
            "name": "Wieacker-Wolff syndrome, female-restricted",
            "description": "Wieacker-Wolff syndrome, female-restricted"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061015"
    ],
    "unlinked_id_list": []
}