Activation-induced cytidine deaminase deficiency (Q85056): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_603312357 | |||
| Property / CURIE: CID11:ID_603312357 / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_603312357
0 references
