Pseudohypoaldosteronism, type 2 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Pseudohypoaldosteronism type 2 (PHA2) is a rare inherited form of hypertension characterized by hyperkalemia, hyperchloremic metabolic acidosis, normal or elevated aldosterone, low renin, and normal renal function. (Orphanet Rare Disease Ontology, Orphanet_757)
External Link http://www.omim.org/entry/145260
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Genes

2 genes associated with the Pseudohypoaldosteronism, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CUL3 cullin 3
KLHL3 kelch-like family member 3