Bile acid CoA:amino acid N-acyltransferase deficiency

MONDO:0100305

Any 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, 0 tagged with Bile acid CoA:amino acid N-acyltransferase deficiency itself.

Where it sits in the disease tree

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