HOXA5, homeobox A5, 3202

N. diseases: 79; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia
0.300 Biomarker phenotype CTD_human [The etiology of congenital diaphragmatic hernia and esophageal atresia: the Hox genes]. 18351244 2007