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primary hyperoxaluria and oxalosis

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n.
An inherited metabolic disorder characterized by the excretion of large amounts of oxalate in the urine and accompanied by nephrocalcinosis, nephrolithiasis, and extrarenal oxalosis.
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The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.

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