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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: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)