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Galactosemia 4

Just diagnosed with Galactosemia 4?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Galactosemia 4, look for clinical trials, and connect with others living with it — all in one place.

Open the full Galactosemia 4 hub →

Overview

Galactosemia 4 is a rare condition. Also known as Galactosemia type IV, Type 4 galactosemia, Type IV galactosemia, GALM deficiency, GALM deficiency galactosemia, Galactose mutarotase deficiency galactosemia, Galactosemia type 4. Tomeko brings together the specialists, research, clinical trials, treatments and community for Galactosemia 4 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:570422 · OMIM 618881 · ICD-10 E74.2 · GARD 0018005

Find care for Galactosemia 4

Authoritative references for Galactosemia 4

Common questions

I was just diagnosed with Galactosemia 4 — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees Galactosemia 4, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for Galactosemia 4?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Galactosemia 4, filtered to your area.

Are there clinical trials for Galactosemia 4?

Tomeko shows live, recruiting studies for Galactosemia 4 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