Medical dictionary. 2011.
pseudohypoaldosteronism type 1 — (PHA1) a hereditary disorder of infancy characterized by severe salt wasting, failure to thrive, and other signs of aldosterone deficiency in association with normal or elevated aldosterone levels, caused by defects in the mineralocorticoid… … Medical dictionary
pseudohypoaldosteronism type 2 — (PHA2) an endocrine abnormality of autosomal dominant inheritance, seen primarily in adults, characterized by hyperkalemia without salt wasting and caused by resistance to the mineralocorticoid effects of aldosterone on tubular potassium… … Medical dictionary
mineralocorticoid resistance — pseudohypoaldosteronism … Medical dictionary
PHA1 — pseudohypoaldosteronism type 1 * * * pseudohypoaldosteronism type 1 … Medical dictionary
PHA2 — pseudohypoaldosteronism type 2 * * * pseudohypoaldosteronism type 2 … Medical dictionary
PHA1 — • pseudohypoaldosteronism type 1 … Dictionary of medical acronyms & abbreviations
PHA2 — • pseudohypoaldosteronism type 2 … Dictionary of medical acronyms & abbreviations
SCNN1A — Sodium channel, nonvoltage gated 1 alpha, also known as SCNN1A, is a human gene.cite web | title = Entrez Gene: SCNN1A sodium channel, nonvoltage gated 1 alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
List of diseases (P) — A list of diseases in the English Wikipedia.DiseasesTOC PaPac Pal* Pachydermoperiostosis * Pachygyria * Pachyonychia congenita Jackson Lawler type * Pacman dysplasia * Paes Whelan Modi syndrome * Paget disease extramammary * Paget disease… … Wikipedia
Sodium-chloride symporter — Solute carrier family 12 (sodium/chloride transporters), member 3 Identifiers Symbols SLC12A3; FLJ96318; NCCT; TSC External IDs … Wikipedia
