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Disorder of glyoxylate metabolism

MONDO:0017703

Also known as: disorder of glyoxylate metabolism

10 clinical trials for this condition and its sub-types.

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Sub-types

Primary hyperoxaluria type 1 (9) Alanine glyoxylate aminotransferase deficiency (0)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Disease of genetic or genomic mechanism (2) Peroxisomal disease (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Peroxisomal single enzyme/protein defect (0)
Trials to join now! 4 Not yet recruiting 1 Not yet finished but already full! 2 Completed 3
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  • New blood test could help kidney patients in israel

    Knowledge-focused Not yet recruiting

    This study aims to validate a blood test for measuring oxalate levels, which is currently not available in Israel. Researchers will compare results from a local lab with an external lab using 50 blood samples. They will also explore how vitamin C levels relate to oxalate in patie…

    Sponsor: Western Galilee Hospital-Nahariya • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:30 UTC

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