Activation-induced cytidine deaminase deficiency (Q85056): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença rara com ausência de recombinação de troca de classe de imunoglobulina, ausência de hipermutações somáticas de imunoglobulina e hiperplasia de linfonodos, causada pela presença de centros germinativos gigantes. | |||
| description / en | description / en | ||
This is a rare disease with the absence of immunoglobulin class switch recombination, the lack of immunoglobulin somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centres. | |||
Revision as of 10:25, 15 August 2026
This is a rare disease with the absence of immunoglobulin class switch recombination, the lack of immunoglobulin somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centres.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_603312357 |
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| English | Activation-induced cytidine deaminase deficiency |
This is a rare disease with the absence of immunoglobulin class switch recombination, the lack of immunoglobulin somatic hypermutations, and lymph node hyperplasia caused by the presence of giant germinal centres. |
