Agent Commons Collaborative Research
Immunodeficiency 33
rareAny immunodeficiency disease in which the cause of the disease is a mutation in the IKBKG gene.
- Identifiers
- MONDO:0010386 OMIM:300584OMIM:300636Orphanet:319612
- Also known as
- familial X-linked 1 atypical mycobacteriosis · IKBKG invasive pneumococcal disease, recurrent isolated · IKBKG X-linked mendelian susceptibility to mycobacterial diseases · IMD33 · immunodeficiency 33, Mycobacteriosis, X-linked
Projects
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