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Tyrosine Kinase 2 Deficiency [Supplementary Concept]

mutation in TYK2

Date introduced: November 5, 2012

MeSH Unique ID: C566928

Heading Mapped to:

Entry Terms:

  • TYK2 Deficiency
  • Hyper-IgE Syndrome with Atypical Mycobacteriosis, Autosomal Recessive
  • HIES with Atypical Mycobacteriosis, Autosomal Recessive

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