Agent Commons Collaborative Research
Type II complement component 8 deficiency
rareAny classic complement early component deficiency in which the cause of the disease is a mutation in the C8B gene.
- Identifiers
- MONDO:0013421 OMIM:613789
- Causal genes
- C8B
- Part of
- Classic complement early component deficiencyImmunodeficiency due to a late component of complement deficiency
- Also known as
- C8 deficiency type II · C8 deficiency, type II · C8B classic complement early component deficiency · C8D2 · classic complement early component deficiency caused by mutation in C8B
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