C9, complement C9, 735

N. diseases: 62; N. variants: 32
Disease: Complement deficiency disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		0.310 GeneticVariation group BEFREE Deficiency of the ninth component of human complement (C9) is the most common complement deficiency in Japan, with an incidence of approximately one homozygote in 1000, but is very rare in other countries. 10083734 1999
CUI: C0272242
Disease: Complement deficiency disease
Complement deficiency disease 		0.310 Biomarker group GENOMICS_ENGLAND Terminal complement component deficiencies in Japan. 10072634 1998