C9, complement C9, 735

N. diseases: 62; N. variants: 32
Disease: Dermatomyositis, Childhood Type ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0263666
Disease: Dermatomyositis, Childhood Type
Dermatomyositis, Childhood Type 		0.300 Biomarker disease CTD_human Hereditary complement (C9) deficiency associated with dermatomyositis. 11359403 2001