Holocarboxylase Synthetase Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase. (Human Disease Ontology, DOID_859)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D028922
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Genes

1 genes/proteins associated with the disease Holocarboxylase Synthetase Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase) 2.88009