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progressive familial intrahepatic 2 Cholestasis

A hereditary autosomal recessive form of intrahepatic cholestasis that is phenotypically similar to progressive familial intrahepatic cholestasis I (OMIM: 211600). Note that progressive familial intrahepatic cholestasis 2 and benign recurrent intrahepatic cholestasis 2 (OMIM: 605479) are allelic disorders caused by mutations in the ABCB11 gene. OMIM: 601847
Also Known As:
Cholestasis, progressive familial intrahepatic 2; Benign recurrent intrahepatic cholestasis 2 (BRIC2); Cholestasis, Benign Recurrent Intrahepatic, 2; Cholestasis, benign recurrent intrahepatic 2; PFIC2 Progressive familial intrahepatic cholestasis type 2; Progressive familial intrahepatic cholestasis 2
Networked: 4 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Experts

1. Briem-Richter, Andrea: 1 article (10/2018)
2. Brinkert, Florian: 1 article (10/2018)
3. Grabhorn, Enke: 1 article (10/2018)
4. Häussinger, Dieter: 1 article (10/2018)
5. Keitel, Verena: 1 article (10/2018)
6. Krebs-Schmitt, Dorothee: 1 article (10/2018)
7. Müller, Ingo: 1 article (10/2018)
8. Pukite, Ieva: 1 article (10/2018)
9. Stindt, Jan: 1 article (10/2018)
10. Sugiyama, Yuichi: 1 article (01/2017)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to progressive familial intrahepatic 2 Cholestasis:
1. Member 11 Subfamily B ATP Binding Cassette TransporterIBA

Therapies and Procedures

1. Therapeutics
2. Liver Transplantation