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GM1 gangliosidosis

Just diagnosed with GM1 gangliosidosis?

You are not alone. Here is where to start: learn the basics, find a specialist or center that sees GM1 gangliosidosis, look for clinical trials, and connect with others living with it — all in one place.

Open the full GM1 gangliosidosis hub →

Overview

GM1 gangliosidosis is a rare condition. Also known as Beta-galactosidase-1 deficiency, GLB1 deficiency, Landing disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for GM1 gangliosidosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:354 · OMIM 230500, 230600, 230650 · ICD-10 E75.1 · GARD 0010891

Find care for GM1 gangliosidosis

Authoritative references for GM1 gangliosidosis

Common questions

I was just diagnosed with GM1 gangliosidosis — what should I do first?

Start by learning the basics from an authoritative source, find a specialist or center that sees GM1 gangliosidosis, and connect with a patient organization. Tomeko brings these together on one hub.

Where can I find a specialist for GM1 gangliosidosis?

Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat GM1 gangliosidosis, filtered to your area.

Are there clinical trials for GM1 gangliosidosis?

Tomeko shows live, recruiting studies for GM1 gangliosidosis 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