Alanine glyoxylate aminotransferase deficiency
MONDO:0100278Any 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
11 clinical trials for this condition and its sub-types, 0 tagged with Alanine glyoxylate aminotransferase deficiency itself.
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Browse by category →Sub-types of Alanine glyoxylate aminotransferase deficiency
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Primary hyperoxaluria type 1 10 trials