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
10 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
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)