primary hyperoxaluria and oxalosis

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