{
    "disease_id": "DOID:0112026", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "intellectual disability, X-linked 99"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "USP9X non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in USP9X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "MRX99"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "mental retardation, X-linked type 99"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "mental retardation, X-linked 99"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010487", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010487", 
            "name": "mental retardation, X-linked 99; MRX99"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112026", 
            "name": "MRX99"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112026", 
            "name": "X-linked mental retardation 99"
        }, 
        {
            "url": "https://www.omim.org/entry/300919", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300919", 
            "name": "Mental retardation, X-linked 99"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112026", 
        "description": "A non-syndromic X-linked intellectual disability characterized by developmental delay, hypotonia, and variable behavioral abnormalities that has_material_basis_in hemizygous mutation in USP9X on chromosome Xp11.4.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112026", 
        "name": "non-syndromic X-linked intellectual disability 99"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300919", 
            "id": "300919", 
            "database": "MIM"
        }
    ]
}