|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital bile acid synthesis defect type 4 (BAS defect type 4) is an anomaly of bile acid synthesis (see this term) characterized by mild cholestatic liver disease, fat malabsorption and/or neurological disease. (Orphanet Rare Disease Ontology, Orphanet_79095)|
|Downloads & Tools|
1 genes associated with the alpha-methylacyl-coa racemase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.