Congenital bile acid synthesis defect type 2 (Q90076): Difference between revisions
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O defeito congênito na síntese do ácido biliar tipo 2 é uma anomalia da síntese do ácido biliar caracterizada por doença hepática colestática grave e rapidamente progressiva acompanhada de má absorção de gordura e vitaminas lipossolúveis. | |||
| description / en | description / en | ||
Congenital bile acid synthesis defect type 2 (BAS defect type 2) is an anomaly of bile acid synthesis characterised by severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins. | |||
Revision as of 17:01, 15 August 2026
Congenital bile acid synthesis defect type 2 (BAS defect type 2) is an anomaly of bile acid synthesis characterised by severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_383380992 |
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| English | Congenital bile acid synthesis defect type 2 |
Congenital bile acid synthesis defect type 2 (BAS defect type 2) is an anomaly of bile acid synthesis characterised by severe and rapidly progressive cholestatic liver disease, and malabsorption of fat and fat-soluble vitamins. |
