SEMA4A, semaphorin 4A, 64218

N. diseases: 141; N. variants: 5
Disease: Familial Colorectal Cancer Type X ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3896578
Disease: Familial Colorectal Cancer Type X
Familial Colorectal Cancer Type X 		0.310 GeneticVariation disease BEFREE Our study shows previously unidentified germline variants in SEMA4A predisposing to FCCTX, which has implications for surveillance strategies of patients and their families. 25307848 2014
CUI: C3896578
Disease: Familial Colorectal Cancer Type X
Familial Colorectal Cancer Type X 		0.310 GermlineCausalMutation disease ORPHANET Our study shows previously unidentified germline variants in SEMA4A predisposing to FCCTX, which has implications for surveillance strategies of patients and their families. 25307848 2014