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