Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (6)
DOID:0050888 - syndromic intellectual disability


Disease Ontology Definition:An intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms.

Synonyms:

Xenbase Genes : arx, igbp1, mecp2, aff2, sms, huwe1, las1l, cul4b, atp6ap2, ube2a, thoc2, med12, eif2s3, hsd17b10, phf8, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000508 - syndromic intellectual disability

OMIM:
OMIM:300486 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL
OMIM:300860 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN
OMIM:309583 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): intellectual disability (is_a)