Medical dictionary. 2011.
Primary hyperoxaluria — Classification and external resources DiseasesDB 6280 Primary hyperoxaluria results in increased excretion of oxalate, with oxalate stones being common. The oxalalate in these common conditions is derived from dietary sources or is secondary to… … Wikipedia
Hyperoxaluria — Classification and external resources Oxalate ICD 10 E … Wikipedia
Hyperoxaluria — An hereditary disorder that causes a special type of stone to form in the kidney and the urine beginning in childhood. Also known as oxalosis. The clinical features of this disease include the following: {{}}Urinary tract: Stones in the urine and … Medical dictionary
type I — primary hyperoxaluria due to deficiency of alanine–glyoxylate transaminase as the result of mutation in the AGXT gene (locus: 2q36 q37) … Medical dictionary
type II — primary hyperoxaluria, milder than type I, caused by mutation in the GRHPR gene (locus: 9cen), resulting in a defect in an enzyme complex involved in the metabolism of hydroxypyruvate to D glycerate … Medical dictionary
PH1 — • primary hyperoxaluria type 1 … Dictionary of medical acronyms & abbreviations
AGXT — Alanine glyoxylate aminotransferase (oxalosis I; hyperoxaluria I; glycolicaciduria; serine pyruvate aminotransferase), also known as AGXT, is a human gene.cite web | title = Entrez Gene: AGXT alanine glyoxylate aminotransferase (oxalosis I;… … Wikipedia
GRHPR — Glyoxylate reductase/hydroxypyruvate reductase, also known as GRHPR, is a human gene.cite web | title = Entrez Gene: GRHPR glyoxylate reductase/hydroxypyruvate reductase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
Kidney stone — Classification and external resources … Wikipedia
oxalosis — Widespread deposition of calcium oxalate crystals in the kidneys, bones, arterial media, and myocardium, with increased urinary excretion of oxalate; may be an acquired disorder, as in oxalate poisoning … Medical dictionary
