| PH | parathyroid hormone; partial hepatectomy; partial hysterectomy; passive hemagglutination; past histo... |
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| PH | Primary hyperoxaluria |
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| PH1 | Primary hyperoxaluria Type 1 |
| hyperoxaluria | A genetic disease of autosomal recessive inheritance that results in the deposition of calcium oxalate in the genitourinary system and kidneys (nephrocalcinosis). Usually evident in the first decade of life, progressive renal failure is not uncommon. Inheritance: autosomal recessive. Origin: Gr. Ouron = urine (27 Sep 1997) |
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| hyperoxaluria, primary | Either of two genetic disorders characterised by urinary excretion of large amounts of oxalate, with nephrolithiasis, nephrocalcinosis, early onset of renal failure, and often a generalised deposit of calcium oxalate, resulting from a defect in glyoxalate metabolism. (12 Dec 1998) |
| primary hyperoxaluria and oxalosis | A metabolic disorder characterised by calcium oxalate nephrocalcinosis and nephrolithiasis, extrarenal oxalosis, and increased urinary output of oxalic and glycolic acids; usually evident clinically in the first decade of life, with progressive renal failure and uraemia; autosomal recessive inheritance. Type I is due to an alteration in alanine:glyoxylate aminotransferase; type II is due to an alteration in d-glycerate dehydrogenase. (05 Mar 2000) |
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Synonyms :
Synonyms : Primary Hyperoxaluria, Primary Oxaluria, Hyperoxalurias, Primary, Oxalurias, Primary, Primary Hyperoxalurias, Primary Oxalurias
| hyperoxaluria |
Abnormally high urine oxalate levels.
출처: www.kidneystonesbook.net/glossary.html
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| hyperoxaluria |
Excretion of excessive amounts of oxalate in the urine.
출처: www.urostonecenter.com/glossary.asp
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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