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Fabry disease

Just diagnosed with Fabry disease?

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

Open the full Fabry disease hub →

Overview

Fabry disease is a rare condition. Also known as Alpha-galactosidase A deficiency, Anderson-Fabry disease, FD. Tomeko brings together the specialists, research, clinical trials, treatments and community for Fabry disease so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:324 · OMIM 301500 · ICD-10 E75.2 · GARD 0006400

Find care for Fabry disease

Authoritative references for Fabry disease

Common questions

I was just diagnosed with Fabry disease — what should I do first?

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

Where can I find a specialist for Fabry disease?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Fabry disease, filtered to your area.

Are there clinical trials for Fabry disease?

Tomeko shows live, recruiting studies for Fabry disease 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