PRSS8, serine protease 8, 5652

N. diseases: 54; N. variants: 0
Disease: Embryopathies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013949
Disease: Embryopathies
Embryopathies 		0.300 Biomarker disease CTD_human Mutations of the serine protease CAP1/Prss8 lead to reduced embryonic viability, skin defects, and decreased ENaC activity. 22705055 2012