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Gaucher disease type I

Just diagnosed with Gaucher disease type I?

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

Open the full Gaucher disease type I hub →

Overview

Gaucher disease type I is a rare condition. Also known as Non-cerebral juvenile Gaucher disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Gaucher disease type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:77259 · OMIM 230800 · ICD-10 E75.2 · GARD 0002441

Find care for Gaucher disease type I

Authoritative references for Gaucher disease type I

Common questions

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

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

Where can I find a specialist for Gaucher disease type I?

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

Are there clinical trials for Gaucher disease type I?

Tomeko shows live, recruiting studies for Gaucher disease type I 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