You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hyper-IgE recurrent infection syndrome 1, autosomal dominant, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hyper-IgE recurrent infection syndrome 1, autosomal dominant hub →Hyper-IgE recurrent infection syndrome 1, autosomal dominant is a rare condition. Also known as AD-HIES due to STAT3 deficiency, Autosomal dominant HIES due to STAT3 deficiency, Autosomal dominant hyperimmunoglobulin E syndrome due to signal transducer and activator of transcription 3 protein deficiency, Buckley syndrome, Job syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hyper-IgE recurrent infection syndrome 1, autosomal dominant so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2314 · OMIM 147060 · ICD-10 D82.4 · GARD 0006800
Start by learning the basics from an authoritative source, find a specialist or center that sees Hyper-IgE recurrent infection syndrome 1, autosomal dominant, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Hyper-IgE recurrent infection syndrome 1, autosomal dominant, filtered to your area.
Tomeko shows live, recruiting studies for Hyper-IgE recurrent infection syndrome 1, autosomal dominant from ClinicalTrials.gov on the hub.