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Infantile glycine encephalopathy

Just diagnosed with Infantile glycine encephalopathy?

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

Open the full Infantile glycine encephalopathy hub →

Overview

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

Identifiers: ORPHA:289860 · OMIM 605899, 620398, 620423 · ICD-10 E72.5 · GARD 0017333

Find care for Infantile glycine encephalopathy

Authoritative references for Infantile glycine encephalopathy

Common questions

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

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

Where can I find a specialist for Infantile glycine encephalopathy?

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

Are there clinical trials for Infantile glycine encephalopathy?

Tomeko shows live, recruiting studies for Infantile 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