Bile acid CoA:amino acid N-acyltransferase deficiency
MONDO:0100305Any disorder of bile acid aminotransferase in which the cause of the disease is a mutation in the BAAT gene.
Also known as: BAAT deficiency, bile acid CoA:amino acid N-acyltransferase deficiency
1 clinical trial for this condition and its sub-types.
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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 bile acid aminotransferase
(0)