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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.

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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.


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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.
Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2020
To see the data from this visualization as text, click here.
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