Mineralocorticoid Excess Syndrome, Apparent Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0342488
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Genes

8 genes associated with the disease Mineralocorticoid Excess Syndrome, Apparent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
KNSTRN kinetochore-localized astrin/SPAG5 binding protein
NR3C2 nuclear receptor subfamily 3, group C, member 2
REN renin
SLC26A3 solute carrier family 26 (anion exchanger), member 3
SLC26A4 solute carrier family 26 (anion exchanger), member 4