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Summary Literature (0)
DOID:9268 - glycine encephalopathy

Disease Ontology Definition:An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues.

Synonyms: GCE, NKH, nonketotic hyperglycinemia, Non-ketotic hyperglycinemia , Non-ketotic hyperglycinemia (disorder)

Xenbase Genes : amt, gcsh, gldc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011612 - glycine encephalopathy


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a), autosomal recessive disease (is_a)