HOXA2, homeobox A2, 3199

N. diseases: 26; N. variants: 3
Disease: Congenital ear anomaly NOS (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266589
Disease: Congenital ear anomaly NOS (disorder)
Congenital ear anomaly NOS (disorder) 		0.010 GeneticVariation group BEFREE Because of the distinct ear anomalies and the hearing loss a HOXA2 mutation was taken into account. 19334086 2009