Disease #02395 (PFIC2 (cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2)), OMIM:601847)

Official abbreviation	PFIC2
Name	cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2)
OMIM ID	601847
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ABCB11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD