{
    "disease_id": "DOID:0060815",
    "recommended_name": {
        "id": "DOID:0060815",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060815",
        "name": "Wieacker-Wolff syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by severe intellectual deficit, microcephaly, exotropia, distal muscle wasting and low digital arches that has_material_basis_in variation in chromosomal region Xq13-q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "MCS",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "MRXS4",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "mental retardation, X-linked, syndromic 4",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "X-linked intellectual disability, Miles-Carpenter type",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "mental retardation, X-linked, with congenital contractures and low fingertip arches",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "Miles-Carpenter syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060815",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060815",
            "name": "WRWF",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker-Wolff syndrome",
            "description": "A severe X-linked recessive neurodevelopmental disorder characterized by severe contractures (arthrogryposis) and intellectual disability."
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "MCS",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "MRXS4",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Miles-CARPENTER X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Miles-Carpenter syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "WRWF",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "WRWFXLR",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker Wolff syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker-Wolff syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker-Wolff syndrome, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "Wieacker-Wolff syndrome, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "X-linked intellectual disability, Miles-Carpenter type",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "ZC4H2-Associated Rare Disorders (ZARD)",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "apraxia, oculomotor, with congenital contractures and muscle atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "contractures of feet, muscle atrophy, and oculomotor apraxia",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "foot contractures-muscle atrophy-oculomotor apraxia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "intellectual disability-developmental delay-contractures syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "mental retardation, X-linked, syndromic 4",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "mental retardation, X-linked, with congenital contractures and Low fingertip arches",
            "description": ""
        },
        {
            "id": "MONDO:0010758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010758",
            "name": "mental retardation, X-linked, with congenital contractures and low fingertip arches",
            "description": ""
        },
        {
            "id": "MIM:314580",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/314580",
            "name": "Wieacker-Wolf syndrome",
            "description": "Wieacker-Wolf syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060815"
    ],
    "unlinked_id_list": []
}