You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Autosomal dominant isolated somatotropin deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Autosomal dominant isolated somatotropin deficiency hub →Autosomal dominant isolated somatotropin deficiency is a rare condition. Also known as Congenital IGHD type II, Congenital isolated GH deficiency type II, Congenital isolated growth hormone deficiency type II. Tomeko brings together the specialists, research, clinical trials, treatments and community for Autosomal dominant isolated somatotropin deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:231679 · OMIM 173100, 613038 · ICD-10 E23.0 · GARD 0001696
Start by learning the basics from an authoritative source, find a specialist or center that sees Autosomal dominant isolated somatotropin deficiency, 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 Autosomal dominant isolated somatotropin deficiency, filtered to your area.
Tomeko shows live, recruiting studies for Autosomal dominant isolated somatotropin deficiency from ClinicalTrials.gov on the hub.