Immunodeficiency 35

Any hereditary predisposition to infections in which the cause of the disease is a mutation in the TYK2 gene.

Also known as: HIES with atypical Mycobacteriosis, autosomal recessive, IMD35, TYK2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency, TYK2 deficiency, autosomal recessive hyper-IgE syndrome due to TYK2 deficiency, autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in TYK2, hyper-IgE syndrome with atypical Mycobacteriosis, autosomal recessive, immunodeficiency 35

0 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 35 itself.