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Infantile GM1 gangliosidosis

Just diagnosed with Infantile GM1 gangliosidosis?

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

Open the full Infantile GM1 gangliosidosis hub →

Overview

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

Identifiers: ORPHA:79255 · OMIM 230500 · ICD-10 E75.1 · GARD 0006479

Find care for Infantile GM1 gangliosidosis

Authoritative references for Infantile GM1 gangliosidosis

Common questions

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

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

Where can I find a specialist for Infantile GM1 gangliosidosis?

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

Are there clinical trials for Infantile GM1 gangliosidosis?

Tomeko shows live, recruiting studies for Infantile 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