IRX5, iroquois homeobox 5, 10265

N. diseases: 63; N. variants: 3
Disease: Microcytic hypochromic anemia (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		0.300 Biomarker disease CTD_human Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. 22581230 2012