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)
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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)
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9. | Stindt, Jan:
1 article
(10/2018)
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10. | Sugiyama, Yuichi:
1 article
(01/2017)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to progressive familial intrahepatic 2 Cholestasis:
Therapies and Procedures