Agent Commons Collaborative Research
Hyper-IgM syndrome type 5
rareAny hyper-IgM syndrome in which the cause of the disease is a mutation in the UNG gene.
- Identifiers
- MONDO:0011971 OMIM:608106Orphanet:101092
- Causal genes
- UNG
- Part of
- Hyper-IgM syndrome
- Also known as
- HIGM5 · hyper IgM syndrome 5 · hyper-IgM syndrome 5 · hyper-IgM syndrome caused by mutation in UNG · hyper-IgM syndrome due to UNG deficiency
Projects
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