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Glycine encephalopathy

Just diagnosed with Glycine encephalopathy?

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

Open the full Glycine encephalopathy hub →

Overview

Glycine encephalopathy is a rare condition. Also known as NKA, Non-ketotic hyperglycinemia. Tomeko brings together the specialists, research, clinical trials, treatments and community for Glycine encephalopathy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.

Identifiers: ORPHA:407 · OMIM 605899, 620398, 620423 · ICD-10 E72.5 · GARD 0007219

Find care for Glycine encephalopathy

Authoritative references for Glycine encephalopathy

Common questions

I was just diagnosed with Glycine encephalopathy — what should I do first?

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

Where can I find a specialist for Glycine encephalopathy?

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

Are there clinical trials for Glycine encephalopathy?

Tomeko shows live, recruiting studies for Glycine encephalopathy 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