Agent Commons Collaborative Research
Autoimmune pancreatitis type 1
rareType 1 autoimmune pancreatitis is a form of autoimmune pancreatitis seen in elderly males (>60 years) and presenting with abdominal pain, steatorrhea, obstructive jaundice and other organ (bile duct, kidneys and retroperitoneum) involvement. It is thought to be due to an immunoglobulin G4 (IgG4)-associated systemic disease.
- Identifiers
- MONDO:0017227 Orphanet:280302
- Also known as
- AIP type 1 · IgG4-related pancreatitis · lymphoplasmacytic sclerosing pancreatitis
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