Details of Disease | DrugMAP

General Information of Disease (ID: DIS3GU4D)

Disease Name	Bile acid malabsorption, primary, 2
Disease Hierarchy	DISYKSRF: Genetic disease DIS3GU4D: Bile acid malabsorption, primary, 2
Disease Identifiers	MONDO ID MONDO_0859180 UMLS CUI C5561962 OMIM ID 619481 MedGen ID 1794172

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC51B	DT1V9AJ	Limited	Unknown	[1]
------------------------------------------------------------------------------------

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
SLC51B	OT4WYPSR	Limited	Unknown	[1]
------------------------------------------------------------------------------------

References

1	Organic solute transporter- (SLC51B) deficiency in two brothers with congenital diarrhea and features of cholestasis. Hepatology. 2018 Aug;68(2):590-598. doi: 10.1002/hep.29516. Epub 2018 May 11.