"Hyperoxaluria, Primary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
| Descriptor ID |
D006960
|
| MeSH Number(s) |
C12.777.419.313.500 C13.351.968.419.313.500 C16.320.565.202.460 C18.452.648.202.460
|
| Concept/Terms |
Hyperoxaluria, Primary- Hyperoxaluria, Primary
- Hyperoxalurias, Primary
- Primary Hyperoxalurias
- Primary Hyperoxaluria
- Primary Oxaluria
- Oxaluria, Primary
- Oxalurias, Primary
- Primary Oxalurias
Primary Oxalosis- Primary Oxalosis
- Oxaloses, Primary
- Oxalosis, Primary
- Primary Oxaloses
|
Below are MeSH descriptors whose meaning is more general than "Hyperoxaluria, Primary".
- Diseases [C]
- Male Urogenital Diseases [C12]
- Urologic Diseases [C12.777]
- Kidney Diseases [C12.777.419]
- Hyperoxaluria [C12.777.419.313]
- Hyperoxaluria, Primary [C12.777.419.313.500]
- Female Urogenital Diseases and Pregnancy Complications [C13]
- Female Urogenital Diseases [C13.351]
- Urologic Diseases [C13.351.968]
- Kidney Diseases [C13.351.968.419]
- Hyperoxaluria [C13.351.968.419.313]
- Hyperoxaluria, Primary [C13.351.968.419.313.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
- Hyperoxaluria, Primary [C16.320.565.202.460]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Metabolism, Inborn Errors [C18.452.648]
- Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
- Hyperoxaluria, Primary [C18.452.648.202.460]
Below are MeSH descriptors whose meaning is more specific than "Hyperoxaluria, Primary".
This graph shows the total number of publications written about "Hyperoxaluria, Primary" by people in this website by year, and whether "Hyperoxaluria, Primary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
| 2013 | 2 | 0 | 2 |
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Below are the most recent publications written about "Hyperoxaluria, Primary" by people in Profiles.
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A 2-month-old female infant with failure to thrive. Pediatr Ann. 2013 May; 42(5):191-3.
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Stroke in primary hyperoxaluria type I. J Neuroimaging. 2014 Jul-Aug; 24(4):411-3.
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Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis. Clin J Am Soc Nephrol. 2011 Sep; 6(9):2289-95.
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Cortical nephrocalcinosis in an infant caused by primary hyperoxaluria type 1. Pediatr Radiol. 2010 Dec; 40 Suppl 1:S13.