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Atypical glycine encephalopathy

Just diagnosed with Atypical glycine encephalopathy?

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

Open the full Atypical glycine encephalopathy hub →

Overview

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

Identifiers: ORPHA:289863 · OMIM 605899, 617301, 620398 · ICD-10 E72.5 · GARD 0017334

Find care for Atypical glycine encephalopathy

Authoritative references for Atypical glycine encephalopathy

Common questions

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

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

Where can I find a specialist for Atypical glycine encephalopathy?

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

Are there clinical trials for Atypical glycine encephalopathy?

Tomeko shows live, recruiting studies for Atypical 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