Familial intrahepatic cholestasis

rare

An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0017290 Orphanet:284385
Part of: Inborn errors of metabolism Intrahepatic cholestasis Liver disorder
Also known as: hereditary intrahepatic cholestasis

Subtypes

Disease	ID	Subtypes	Genes
Progressive familial intrahepatic cholestasis	MONDO:0015762	16
Benign recurrent intrahepatic cholestasis	MONDO:0019008	3
Cholestasis, intrahepatic, of pregnancy, 1	MONDO:0007829		ATP8B1
Cholestasis, intrahepatic, of pregnancy, 3	MONDO:0013995		ABCB4

Rare disease

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