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Neonatal glycine encephalopathy

Just diagnosed with Neonatal glycine encephalopathy?

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

Open the full Neonatal glycine encephalopathy hub →

Overview

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

Identifiers: ORPHA:289857 · OMIM 605899, 620398, 620423 · ICD-10 E72.5 · GARD 0017332

Find care for Neonatal glycine encephalopathy

Authoritative references for Neonatal glycine encephalopathy

Common questions

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

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

Where can I find a specialist for Neonatal glycine encephalopathy?

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

Are there clinical trials for Neonatal glycine encephalopathy?

Tomeko shows live, recruiting studies for Neonatal 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