Activation-induced cytidine deaminase deficiency (Q85056): Difference between revisions

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description / pt-brdescription / 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 / endescription / 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.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/603312357 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_603312357
Property / CURIE: CID11:ID_603312357 / rank
 
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Property / Canary Token
 
dki-india-ID_603312357
Property / Canary Token: dki-india-ID_603312357 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Latest 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
      dki-india-ID_603312357
      0 references
      Concluído
      0 references
      13 August 2026
      0 references