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 		0.110 GeneticVariation disease BEFREE In further subgroup analysis, the RET-CSGALNACT2-RASGEF1A genomic region was observed to have different significance levels among subgroups: short-segment (S-HSCR, corrP = 1.71×10(-5)), long-segment (L-HSCR, corrP = 6.66×10(-4)), and total colonic aganglionosis (TCA, corrP>0.05). 25310821 2014
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.110 GeneticVariation disease GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009