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autoimmune pancreatitis

Disease Summary
Associated Targets (0)

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Mondo Description Autoimmune pancreatitis (AIP) is a rare pancreatic disease characterized by chronic non-alcoholic pancreatitis that presents with abdominal pain, steatorrhea, obstructive jaundice and responds well to steroid therapy and is seen in two subforms: type 1 AIP which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 AIP which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels.
Mondo Term and Equivalent IDs
MONDO:0015175:  autoimmune pancreatitis
GARD:0010911: 
Orphanet:103919: 
SCTID:448542008: 
UMLS:C2609129: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found