 Hyperoxaluria, Primary
"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
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| MeSH Number(s) |
C12.777.419.313.500 C13.351.968.419.313.500 C16.320.565.202.460 C18.452.648.202.460
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| Concept/Terms |
Hyperoxaluria, Primary- Hyperoxaluria, Primary
- Primary Hyperoxaluria
- Hyperoxalurias, Primary
- Primary Hyperoxalurias
- Primary Oxaluria
- Oxalurias, Primary
- Primary Oxalurias
- Oxaluria, Primary
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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 UAMS Profiles by year, and whether "Hyperoxaluria, Primary" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2022 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Hyperoxaluria, Primary" by people in Profiles over the past ten years.
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Ly S, Rick J, Goff R, David BA, Kincannon J, Shalin S. Cutaneous Oxalosis Due to Primary Hyperoxaluria. Am J Dermatopathol. 2022 Dec 01; 44(12):981-983.
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Shah RJ, Vaughan LE, Enders FT, Milliner DS, Lieske JC. Plasma Oxalate as a Predictor of Kidney Function Decline in a Primary Hyperoxaluria Cohort. Int J Mol Sci. 2020 May 20; 21(10).
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