holocarboxylase synthetase deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase. (Human Disease Ontology, DOID_859)
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9 genes co-occuring with the disease holocarboxylase synthetase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase) 3.01585
BTD biotinidase 1.85228
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase 1.13839
PC pyruvate carboxylase 1.13036
HADH hydroxyacyl-CoA dehydrogenase 0.869187
AGL amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase 0.826999
PTS 6-pyruvoyltetrahydropterin synthase 0.757786
MUT methylmalonyl CoA mutase 0.666755
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 0.187719