Primary Biliary Cholangitis (PBC)

Alias:

Primary Biliary Cirrhosis

Hanot Syndrome

Chronic Nonsuppurative Destructive Cholangitis

Biliary Liver Cirrhosis

Pbc

Familial Primary Biliary Cirrhosis

Pericholangiolic Biliary Cirrhosis

Tannhauser-Magendantz Syndrome

Hypertrophic Biliary Cirrhosis

Xanthomatous Biliary Cirrhosis

Biliary Cirrhosis Primary

Mahon-Tannhauser Syndrome

Liver Cirrhosis, Biliary

Hypertrophic Cirrhosis

Cholestatic Cirrhosis

Hanot-Rossle Syndrome

Monolobular Cirrhosis

Unilobar Cirrhosis

Hanot's Cirrhosis

Biliary Cirrhosis

Charcot Cirrhosis

Hanot Cirrhosis

Toxic Cirrhosis

Todd Cirrhosis

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Primary Biliary Cholangitis, also known as primary biliary cirrhosis, is related to steatotic liver disease and systemic lupus erythematosus. An important gene associated with Primary Biliary Cholangitis is PBC2 (Biliary Cirrhosis, Primary, 2), and among its related pathways/superpathways are miRNAs involved in DNA damage response and Cell differentiation - expanded index. The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include Umbilical Cord, liver and bone, and related phenotypes are cirrhosis and biliary cirrhosis

Related ID：

MALACARDS：PRM236

MESH：D008105

ICD11：649193479