Hyper-IgM syndrome due to uracil N glycosylase (Q85054): Difference between revisions
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Revision as of 10:24, 15 August 2026
This has been characterised in three patients from France and Japan. The symptoms are similar to hyper IgM syndrome type 2, but the AICDA gene is intact.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_492472329 |
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| English | Hyper-IgM syndrome due to uracil N glycosylase |
This has been characterised in three patients from France and Japan. The symptoms are similar to hyper IgM syndrome type 2, but the AICDA gene is intact. |
