C9, complement C9, 735

N. diseases: 62; N. variants: 32
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0041834
Disease: Erythema
Erythema
0.300 Biomarker phenotype CTD_human Hereditary complement (C9) deficiency associated with dermatomyositis. 11359403 2001