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Disease association ontology term - MONDO:0011612 - glycine encephalopathy

Term summary

ID
MONDO:0011612
Name
glycine encephalopathy
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0011612 - glycine encephalopathy

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MONDO:0958179 - glycine encephalopathy 1

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MONDO:0958192 - glycine encephalopathy 2

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MONDO:0957382 - multiple mitochondrial dysfunctions syndrome 7

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