glycine encephalopathy

Summary
Synonym
  • Non-ketotic hyperglycinemia
  • nonketotic hyperglycinemia
Definition
An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues.
Super Class
amino acid metabolic disorder
Disease Ontology
DOID:9268
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
275 AMT aminomethyltransferase
2653 GCSH glycine cleavage system protein H
2731 GLDC glycine decarboxylase
6536 SLC6A9 solute carrier family 6 member 9
Displaying 1 entry
Gene ID Gene Symbol Description Source
104174 Gldc glycine decarboxylase
Displaying 1 entry
Gene ID Gene Symbol Description Source
116509 Slc6a9 solute carrier family 6 member 9
Displaying 1 entry
Gene ID Gene Symbol Description Source
37772 GlyT Glycine transporter
The Human Phenotype Ontology
Displaying entries 1 - 10 of 20 in total
HPO ID HPO Term
HP:0001252 Hypotonia
HP:0001522 Death in infancy
HP:0000737 Irritability
HP:0100710 Impulsivity
HP:0001290 Generalized hypotonia
HP:0000711 Restlessness
HP:0001336 Myoclonus
HP:0001249 Intellectual disability
HP:0003108 Hyperglycinuria
HP:0001265 Hyporeflexia
Displaying 1 entry
Gene ID Gene Symbol Description
2731 GLDC glycine decarboxylase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024