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Summary Literature (3)
DOID:0060307 - autosomal dominant non-syndromic intellectual disability

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

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

In Mondo Disease Ontology:
MONDO:0015802 - autosomal dominant non-syndromic intellectual disability

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): non-syndromic intellectual disability (is_a)