SEMA3C, semaphorin 3C, 10512

N. diseases: 71; N. variants: 4
Disease: Congenital Intestinal Aganglionosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3661523
Disease: Congenital Intestinal Aganglionosis
Congenital Intestinal Aganglionosis 		0.300 SusceptibilityMutation disease ORPHANET Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. 25839327 2015