{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "intellectual disability, X-linked 30"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "mental retardation, X-linked type 30"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "MRX30"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "mental retardation, X-linked 30"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "mental retardation, X-linked 47"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in PAK3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "PAK3 non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010361", 
            "name": "mental retardation, X-linked 30; MRX30"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050776", 
            "name": "non-specific X-linked mental retardation"
        }, 
        {
            "url": "https://www.omim.org/entry/300558", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300558", 
            "name": "Mental retardation, X-linked 30"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050776", 
        "description": "A non-syndromic intellectual disability characterized by a X-linked inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050776", 
        "name": "non-syndromic X-linked intellectual disability"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300558", 
            "id": "300558", 
            "database": "MIM"
        }
    ]
}