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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
Neurofibromatosis type I — For Von Recklinghausen s disease of bone, a disorder seen with hyperparathyroidism, see osteitis fibrosa cystica. Neurofibromatosis type 1 Classification and external resources ICD 10 Q85.0 (ILDS Q85.010) ICD … Wikipedia
Neurofibromatosis type II — Classification and external resources ICD 10 D33, Q85.0 (ILDS Q85.020) ICD 9 … Wikipedia
Mucolipidosis type IV — Classification and external resources ICD 10 E75.1 OMIM 252650 DiseasesDB … Wikipedia
PHA1 — • pseudohypoaldosteronism type 1 … Dictionary of medical acronyms & abbreviations
PHA2 — • pseudohypoaldosteronism type 2 … Dictionary of medical acronyms & abbreviations
PHA1 — pseudohypoaldosteronism type 1 * * * pseudohypoaldosteronism type 1 … Medical dictionary
PHA2 — pseudohypoaldosteronism type 2 * * * pseudohypoaldosteronism type 2 … Medical dictionary
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
