You are not alone. Here is where to start: learn the basics, find a specialist or center that sees X-linked agammaglobulinemia with growth hormone deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full X-linked agammaglobulinemia with growth hormone deficiency hub →X-linked agammaglobulinemia with growth hormone deficiency is a rare condition. Also known as Congenital IGHD type III, Congenital isolated GH deficiency type III, Congenital isolated growth hormone deficiency type III, X-linked IGHD, X-linked isolated growth hormone deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for X-linked agammaglobulinemia with growth hormone deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:231692 · OMIM 300123, 307200 · ICD-10 E23.0 · GARD 0003921
Start by learning the basics from an authoritative source, find a specialist or center that sees X-linked agammaglobulinemia with growth hormone 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 X-linked agammaglobulinemia with growth hormone deficiency, filtered to your area.
Tomeko shows live, recruiting studies for X-linked agammaglobulinemia with growth hormone deficiency from ClinicalTrials.gov on the hub.