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susceptibility to infection due to TYK2 deficiency

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency in which the cause of the disease is a mutation in the TYK2 gene.
Uniprot Description A primary immunodeficiency characterized by recurrent skin abscesses, pneumonia, and highly elevated serum IgE.
Mondo Term and Equivalent IDs
MONDO:0012682:  susceptibility to infection due to TYK2 deficiency
MESH:C566928: 
Orphanet:331226: 
UMLS:C1969086: