Hyper-IgM syndrome due to uracil N glycosylase (Q85054): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Foi descrito em três pacientes da França e do Japão. Os sintomas são semelhantes à síndrome de Hiper IgM tipo 2, mas o gene AICDA está intacto. | |||
| description / en | description / en | ||
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. | |||
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. |
