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46,XY partial gonadal dysgenesis

Just diagnosed with 46,XY partial gonadal dysgenesis?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 46,XY partial gonadal dysgenesis, look for clinical trials, and connect with others living with it — all in one place.

Open the full 46,XY partial gonadal dysgenesis hub →

Overview

46,XY partial gonadal dysgenesis is a rare condition. Also known as 46,XY PGD, 46,XY partial testicular dysgenesis. Tomeko brings together the specialists, research, clinical trials, treatments and community for 46,XY partial gonadal dysgenesis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:251510 · OMIM 154230, 300018, 612965 · ICD-10 Q56.1 · GARD 0017211

Find care for 46,XY partial gonadal dysgenesis

Authoritative references for 46,XY partial gonadal dysgenesis

Common questions

I was just diagnosed with 46,XY partial gonadal dysgenesis — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees 46,XY partial gonadal dysgenesis, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for 46,XY partial gonadal dysgenesis?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 46,XY partial gonadal dysgenesis, filtered to your area.

Are there clinical trials for 46,XY partial gonadal dysgenesis?

Tomeko shows live, recruiting studies for 46,XY partial gonadal dysgenesis from ClinicalTrials.gov on the hub.

Informational only — not medical advice. Always consult a qualified clinician. Provider and reference data from public sources (NIH GARD, Orphanet, OMIM, HPO, MONDO, ClinicalTrials.gov, CMS NPPES). © Tomeko · tomekohealth.com