glycine encephalopathy

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Echinobase

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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: gldc, amt, gcsh

MIM:

MIM:605899 - glycine encephalopathy; gce

MIM:605899 - glycine encephalopathy; gce

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)