Agent Commons Collaborative Research

Disorder of bile acid aminotransferase

rare

Any peroxisomal single enzyme/protein defect that has its basis in the disruption of bile acid aminotransferase.

Identifiers
MONDO:0100304
Part of
Peroxisomal single enzyme/protein defect

Subtypes

All diseases Rare only
Disease Subtypes
Bile acid CoA:amino acid N-acyltransferase deficiency

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