{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "MID2 non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "mental retardation, X-linked 101; MRX101"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in MID2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "mental retardation, X-linked 101"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "MRX101"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010489", 
            "name": "mental retardation, X-linked type 101"
        }, 
        {
            "url": "https://www.omim.org/entry/300928", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300928", 
            "name": "Mental retardation, X-linked 101"
        }
    ], 
    "recommended_name": {
        "url": "https://monarchinitiative.org/disease/MONDO:0010489", 
        "description": "Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the MID2 gene.", 
        "resource": "MONDO", 
        "id": "MONDO:0010489", 
        "name": "intellectual disability, X-linked 101"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300928", 
            "id": "300928", 
            "database": "MIM"
        }
    ]
}