autosomal dominant intellectual developmental disorder

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: 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

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)