Glycine encephalopathy (GE) is an inborn error of glycine metabolism characterized by accumulation of glycine in body fluids and tissues, including the brain, resulting in neurometabolic symptoms of variable severity.

Synonyms: Non-ketotic hyperglycinemia NKA

This is just here as a test because I lose it

Term information

database cross reference
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OMIM:605899

UMLS:C0751748

ICD-10:E72.5

notation

ORPHA:407