Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Autosomal dominant disease · Hyper-IgE syndrome
Hyper-IgE recurrent infection syndrome 1, autosomal dominant
A condition of decreased or absent presence or activity of signal transducer and activator of transcription 3 protein. Deficiency of this protein is associated with hyper-IgE syndrome.
This condition has no sub-types.