Disease #00035 (GCE (encephalopathy, glycine (GCE)), OMIM:605899)

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	Curator: Johan T. den Dunnen

Official abbreviation	GCE
Name	encephalopathy, glycine (GCE)
OMIM ID	605899
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	AMT, GCSH, GLDC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-30 16:13:48 +02:00 (CEST)
Date last edited	N/A