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 (4)
DOID:0060307 - autosomal dominant intellectual developmental disorder

Disease Ontology Definition:A intellectual disability characterized by an autosomal dominant inheritance pattern.

Synonyms: autosomal dominant mental retardation, autosomal dominant non-syndromic mental retardation,

Xenbase Genes : sox4, tbl1xr1, smarce1, sox11, smarca4, hivep2, mef2c, ctnnb1, syngap1, csnk2b, rac1, rab11a, smarcc2, arid1a, smarcb1, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015802 - autosomal dominant non-syndromic intellectual disability

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), intellectual disability (is_a), non-syndromic intellectual disability (is_a)