{
    "disease_id": "DOID:0080242",
    "recommended_name": {
        "id": "DOID:0080242",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080242",
        "name": "syndromic X-linked mental retardation Hough type",
        "description": "A syndromic X-linked intellectual disability that is characterized by delayed development, intellectual disability, speech and language delay, and early-onset seizures and that has_material_basis_in hemizygous or heterozygous mutation in the CNKSR2 gene on chromosome Xp22."
    },
    "synonyms": [
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "intellectual disability, X-linked, syndromic, Houge type",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "intellectual developmental disorder, X-linked, syndromic, Houge type",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "intellectual disability, X-linked, syndromic, Houge type",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "MRXSHG",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "mental retardation, X-linked, syndromic, HOUGE type",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "mental retardation, X-linked, syndromic, Houge type",
            "description": ""
        },
        {
            "id": "MONDO:0030909",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030909",
            "name": "syndromic X-linked mental retardation Hough type",
            "description": ""
        },
        {
            "id": "MIM:301008",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301008",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Houge type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Houge type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080242"
    ],
    "unlinked_id_list": []
}