You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 46 XX gonadal dysgenesis, look for clinical trials, and connect with others living with it — all in one place.
Open the full 46 XX gonadal dysgenesis hub →46 XX gonadal dysgenesis is a rare condition. Also known as 46,XX complete gonadal dysgenesis, 46,XX ovarian dysgenesis, 46,XX pure gonadal dysgenesis, Hypergonadotropic ovarian dysgenesis, XX female gonadal dysgenesis, XX-GD. Tomeko brings together the specialists, research, clinical trials, treatments and community for 46 XX gonadal dysgenesis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:243 · OMIM 233300, 300510, 614324 · ICD-10 Q99.1 · GARD 0005671
Start by learning the basics from an authoritative source, find a specialist or center that sees 46 XX gonadal dysgenesis, 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 46 XX gonadal dysgenesis, filtered to your area.
Tomeko shows live, recruiting studies for 46 XX gonadal dysgenesis from ClinicalTrials.gov on the hub.