RELN, reelin, 5649

N. diseases: 178; N. variants: 52
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 Biomarker disease BEFREE We provide a first indication that common variants of GABRG2, RELN and NRG3 and the GABRG2-RELN-PTCH1 interaction networks might confer altered susceptibility to HSCR in the Han Chinese population, suggesting a potential mechanism underlying HSCR pathogenesis. 27889765 2016
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.310 Biomarker disease GENOMICS_ENGLAND Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease. 27889765 2016