|Name||Pseudohypoaldosteronism type II (gene A)|
|Description||Pseudohypoaldosteronism type II, also known as Gordon hyperkalemia-hypertension syndrome, is characterized by hyperkalemia despite normal renal glomerular filtration, hypertension, and correction of physiologic abnormalities by thiazide diuretics. Mild hyperchloremia, metabolic acidosis, and suppressed plasma renin activity are variable associated findings.[supplied by OMIM, Jul 2002]|
|NCBI Gene ID||7830|
|Expression in Tissues and Cell Lines||
PHA2A has 3 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, gene, protein or microRNA) extracted from 3 datasets.
Click the + buttons to view associations for PHA2A from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with PHA2A gene/protein from the curated CTD Gene-Disease Associations dataset.|
|Hub Proteins Protein-Protein Interactions||interacting hub proteins for PHA2A from the curated Hub Proteins Protein-Protein Interactions dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with PHA2A gene from the curated OMIM Gene-Disease Associations dataset.|