{
    "disease_id": "DOID:0060823", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "mental retardation, X-linked, syndromic, Wu type; MRXSW"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "mental retardation, X-linked 94"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "syndromic X-linked intellectual disability type 94"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "mental retardation, X-linked, syndromic, Wu type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "MRX94"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "syndromic X-linked intellectual disability due to GRIA3 anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "MRXSW"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "syndromic X-linked mental retardation 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "syndromic X-linked mental retardation Wu type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "MRXS29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010402", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010402", 
            "name": "mental retardation, X-linked, syndromic 29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "syndromic X-linked intellectual disability due to GRIA3 anomalies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "MRX94"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "MRXS29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "mental retardation, X-linked 94"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "syndromic X-linked mental retardation 29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060823", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060823", 
            "name": "syndromic X-linked mental retardation Wu type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060823", 
        "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has_material_basis_in mutation in the GRIA3 gene on chromosome Xq25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060823", 
        "name": "syndromic X-linked intellectual disability 94"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060823#disease-associations", 
            "id": "0060823", 
            "database": "Alliance of Genome Resources"
        }
    ]
}