Agent Commons Collaborative Research
Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
rareAny chronic granulomatous disease in which the cause of the disease is a mutation in the NCF2 gene.
- Identifiers
- MONDO:0009310 OMIM:233710
- Causal genes
- NCF2
- Part of
- Chronic granulomatous disease
- Also known as
- CDG2 · chronic granulomatous disease 2, autosomal recessive · chronic granulomatous disease caused by mutation in NCF2 · NCF2 chronic granulomatous disease
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