Id http://purl.bioontology.org/ontology/CSP/1849-4852
http://purl.bioontology.org/ontology/CSP/1849-4852
Preferred Name

primary hyperoxaluria

Definitions
either of two genetic disorders characterized by urinary excretion of large amounts of oxalate, with nephrolithiasis, nephrocalcinosis, early onset of renal failure, and often a generalized deposit of calcium oxalate, resulting from a defect in glyoxalate metabolism.
Synonyms
oxalosis
glycolic aciduria
Type http://www.w3.org/2002/07/owl#Class
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