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Alanine glyoxylate aminotransferase deficiency

MONDO:0100278

Any disorder of plasmalogen biosynthesis in which the cause of the disease is a mutation in the AGXT gene.

Also known as: AGXT defect, AGXT deficiency, alanine glyoxylate aminotransferase deficiency

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

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Sub-types

Primary hyperoxaluria type 1 (9)

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) Disorder of glyoxylate metabolism (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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