Bartter syndrome, type 3 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Classic Bartter syndrome is a type of Bartter syndrome (see this term), characterized by a milder clinical picture than the antenatal/infantile subtype, and presenting with failure to thrive, hypokalemic alkalosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II. (Orphanet Rare Disease Ontology, Orphanet_93605)
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1 genes/proteins associated with the disease Bartter syndrome, type 3 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CLCNKB chloride channel, voltage-sensitive Kb 2.88009