steroid inherited metabolic disorder Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lipid metabolism disorder that involves defects in steroid metabolism. (Human Disease Ontology, DOID_1701)
Similar Terms
Downloads & Tools

Genes

9 genes co-occuring with the disease steroid inherited metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2 2.06578
NR3C2 nuclear receptor subfamily 3, group C, member 2 1.65879
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1 1.19834
REN renin 1.14985
HSD17B6 hydroxysteroid (17-beta) dehydrogenase 6 1.13755
CLCNKB chloride channel, voltage-sensitive Kb 0.774523
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1 0.622183
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 0.574994
POMC proopiomelanocortin 0.562946