{
    "disease_id": "DOID:0080242", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030909", 
            "name": "intellectual disability, X-linked, syndromic, Houge type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030909", 
            "name": "mental retardation, X-linked, syndromic, HOUGE type; MRXSHG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030909", 
            "name": "MRXSHG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030909", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030909", 
            "name": "mental retardation, X-linked, syndromic, Houge type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080242", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080242", 
        "name": "syndromic X-linked mental retardation Hough type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080242#disease-associations", 
            "id": "0080242", 
            "database": "Alliance of Genome Resources"
        }
    ]
}