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Congenital bile acid synthesis "defect," type 2
- Congenital bile acid synthesis defect type 2 is a disorder characterized by cholestasis, a condition that impairs the production and release of a digestive fluid ...
- ... the AKR1D1 gene have been found to cause congenital bile acid synthesis defect type 2. This condition is characterized by cholestasis, a condition ... absorbed, leading to the signs and symptoms of congenital bile acid synthesis defect type 2. More About This Health Condition 3-oxo-5- ...
- Liver Diseases (National Library of Medicine)Your liver is the largest organ inside your body. It helps your body digest food, store energy, and remove poisons. There are many kinds of liver diseases: ...
- ... of the same disorder. Because most individuals with congenital bile acid synthesis defect type 4 do not survive infancy, it is unclear whether they would have later developed the neurological symptoms seen in adults with AMACR deficiency. 2-methylacyl-CoA racemase AMACR_HUMAN AMACRD CBAS4 RACE ...
- ... the HSD3B7 gene have been found to cause congenital bile acid synthesis ... mutations delete one or two DNA building blocks (base pairs) from the gene ...
- ... medicines, such as lithium and amiodarone, and some types of chemotherapy Congenital (birth) defects Radiation treatments to the neck or brain to ...
- Definitions of Digestive Terms (International Foundation for Gastrointestinal Disorders)Stomach Disorders/Reference Desk ... Stomach Disorders ... Digestive Diseases/Reference Desk ... Digestive Diseases ... International Foundation for Gastrointestinal Disorders
