C7

PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
C7 deficiency, 610102, Complement component 7 deficiency, Susceptibility to invasive bacterial infection, especially meningococcal, Disseminated neisserial infections, Complement Deficiencies