{
    "disease_id": "DOID:0080241", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030908", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030908", 
            "name": "intellectual disability, X-linked, syndromic, 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030908", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030908", 
            "name": "MRXS35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030908", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030908", 
            "name": "mental retardation, X-linked, syndromic, 35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030908", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030908", 
            "name": "mental retardation, X-linked, syndromic, 35; MRXS35"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080241", 
        "description": "A syndromic X-linked intellectual disability that has_material_basis_in mutation in the RPL10 gene on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080241", 
        "name": "syndromic X-linked mental retardation 35"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080241#disease-associations", 
            "id": "0080241", 
            "database": "Alliance of Genome Resources"
        }
    ]
}