Disorder of bile acid aminotransferase
MONDO:0100304Any peroxisomal single enzyme/protein defect that has its basis in the disruption of bile acid aminotransferase.
Also known as: disorder of bile acid aminotransferase
1 clinical trial for this condition and its sub-types.
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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)