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: C0011633
Disease: Dermatomyositis
Dermatomyositis
0.310 Biomarker disease CTD_human Hereditary complement (C9) deficiency associated with dermatomyositis. 11359403 2001
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis
0.310 GeneticVariation disease BEFREE Hereditary complement (C9) deficiency associated with dermatomyositis. 11359403 2001