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Cholestasis, progressive familial intrahepatic 1 [Supplementary Concept]

A heterogeneous group of hereditary liver disorders characterized by the early onset of CHOLESTASIS that progresses to hepatic FIBROSIS; LIVER CIRRHOSIS, and END-STAGE LIVER DISEASE before adulthood. Germline mutations in the ATP8B1 gene have been identified. OMIM: 211600

Date introduced: August 25, 2010

MeSH Unique ID: C535933

Heading Mapped to:

Entry Terms:

  • Progressive familial intrahepatic cholestasis
  • Cholestasis, fatal intrahepatic
  • Byler's disease
  • Byler disease
  • Cholestasis, Progressive Familial Intrahepatic, 1
  • Progressive familial intrahepatic cholestasis type 1 (PFIC1)
  • FIC1 deficiency
  • Progressive familial intrahepatic cholestasis type 1 (PFIC 1)
  • PFIC1 Progressive familial intrahepatic cholestasis type 1
  • Summerskill syndrome
  • Cholestasis, benign recurrent intrahepatic 1
  • Cholestasis, Benign Recurrent Intrahepatic, 1

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