Alkalosis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Depletion of acid or accumulation base in the body fluids. (Human Phenotype Ontology, HP_0001948)
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Genes

1 genes associated with the Alkalosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3