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Orphanet References OMIM Gene GeneReviews HGMD HGNC
last update : 22/06/2006
Symbol C9
Location 5p13
Name complement component 9 deficiency
Other name(s) C9 deficiency
Corresponding gene C9
related resource C9base - Mutation registry for C9 deficiency
Main clinical features rare episodes of neisserial or meningococcal meningitis
Genetic determination
Related entries C9 deficiency with dermatomyositis
Function/system disorder defense and immunity
Type disease