{
    "disease_id": "DOID:0112045", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "intellectual disability, X-linked 93"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "mental retardation, X-linked type 93"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "MRX93"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "mental retardation, X-linked 93"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "BRWD3 non-syndromic X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "mental retardation, X-linked, with macrocephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "mental retardation, X-linked 93; MRX93"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010393", 
            "name": "non-syndromic X-linked intellectual disability caused by mutation in BRWD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112045", 
            "name": "MRX93"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112045", 
            "name": "X-linked mental retardation 93"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112045", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112045", 
            "name": "X-linked mental retardation with macrocephaly"
        }, 
        {
            "url": "https://www.omim.org/entry/300659", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300659", 
            "name": "Mental retardation, X-linked 93"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112045", 
        "description": "A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability and macrocephaly that has_material_basis_in hemizygous mutation in BRWD3 on chromosome Xq21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112045", 
        "name": "non-syndromic X-linked intellectual disability 93"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300659", 
            "id": "300659", 
            "database": "MIM"
        }
    ]
}