hypoglycemic encephalopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Brain damage related to a lowering of blood glucose below a critical level (around 30 mg/dl), which may lead to confusion, lethargy and delirium followed by seizures and coma. Prolonged hypoglycemia may lead to irreversible brain damage. (Human Phenotype Ontology, HP_0006929)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006929
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Genes

1 genes associated with the hypoglycemic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HADH hydroxyacyl-CoA dehydrogenase