IRX5, iroquois homeobox 5, 10265

N. diseases: 63; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.300 Biomarker group CTD_human Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. 22581230 2012