Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 6.12 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes C9 deficiency, 613825, Complement component 9 deficiency, Susceptibility to invasive bacterial infection, especially meningococcal, Mild susceptibility to disseminated neisserial infections, Complement Deficiencies |