OMOP Concept 1449222

Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency

StandardConditionSNOMED1351570003Disorder
Maps from
0
Descendants
0
Valid from
1 Nov 2024
Valid to
31 Dec 2099
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Synonyms

Alternative names recorded for Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency across source vocabularies.

  • Autosomal dominant activation-induced cytidine deaminase deficiency
  • Autosomal dominant hyper IgM syndrome due to AICDA
  • Autosomal dominant hyper-IgM syndrome type 2
  • Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
  • Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)
  • síndrome de hiper-IgM autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación
  • síndrome de hiperinmunoglobulina M autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación
  • síndrome de hiperinmunoglobulina M autosómico dominante debido a deficiencia de citidina desaminasa inducida por activación (trastorno)

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Ordered by distance - 1 is a direct parent or child.

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