C9, complement C9, 735

N. diseases: 62; N. variants: 32
Disease: Favre-Racouchot Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015704
Disease: Favre-Racouchot Syndrome
Favre-Racouchot Syndrome 		0.300 Biomarker disease CTD_human Hereditary complement (C9) deficiency associated with dermatomyositis. 11359403 2001