isovaleric acidemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An organic acidemia that disrupts or prevents normal metabolism of the branched-chain amino acid leucine. (Human Disease Ontology, DOID_14753)
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Genes

19 genes co-occuring with the disease isovaleric acidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
IVD isovaleryl-CoA dehydrogenase 2.9706
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase 1.76592
ACADSB acyl-CoA dehydrogenase, short/branched chain 1.7623
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain 1.21522
MMD monocyte to macrophage differentiation-associated 1.18238
PCCB propionyl CoA carboxylase, beta polypeptide 0.959123
ACADVL acyl-CoA dehydrogenase, very long chain 0.826178
HADH hydroxyacyl-CoA dehydrogenase 0.687491
ATP11A ATPase, class VI, type 11A 0.626888
OTC ornithine carbamoyltransferase 0.566054
PC pyruvate carboxylase 0.556732
HPX hemopexin 0.524588
MUT methylmalonyl CoA mutase 0.458996
CS citrate synthase 0.410535
CAST calpastatin 0.409787
FGD1 FYVE, RhoGEF and PH domain containing 1 0.397843
LAP3 leucine aminopeptidase 3 0.321909
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial 0.300533
DNAH8 dynein, axonemal, heavy chain 8 0.274021