OMOP Concept 1449226

Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency

StandardConditionSNOMED1351576009Disorder
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 recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency across source vocabularies.

  • Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency
  • Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (disorder)
  • Autosomal recessive hyperimmunoglobulin M syndrome due to mutS homolog 6 deficiency
  • Hyper IgM syndrome due to MSH6
  • síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de MSH6
  • síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de mutador S homólogo 6
  • síndrome de hiperinmunoglobulina M autosómico recesivo debido a deficiencia de mutador S homólogo 6 (trastorno)

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