GAP43, growth associated protein 43, 2596

N. diseases: 109; N. variants: 0
Disease: Hirschsprung Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.310 GeneticVariation disease BEFREE Our study for the first time indicates that genetic variants within GAL, GAP43 and NRSN1 and related gene-gene interaction networks might be involved in the altered susceptibility to HSCR in the Han Chinese population, which might shed more light on HSCR pathogenesis. 29654647 2018
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.310 Biomarker disease GENOMICS_ENGLAND Identification of novel genes in Hirschsprung disease pathway using whole genome expression study. 22325380 2012