Autoimmune Pancreatitis

Watchlist

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

PRSS1, HLA-DRB1, CFTR, ABCF1, AMY2A, FOXP3, SMUG1, CXCL8, SPINK1, PKD1, MED1, PPBP, SCT, CCL11, SKI, AIP, TLR4, ATP8, ABCG2, KNTC1, PDPN, TNFSF13B, MAGT1, IL33, RBM45, PEBP1, LTA, MST1, LTBR, ALPP

PRSS1, HLA-DRB1, CFTR, ABCF1, AMY2A, FOXP3, SMUG1, CXCL8, SPINK1, PKD1, MED1, PPBP, SCT, CCL11, SKI, AIP, TLR4, ATP8, ABCG2, KNTC1, PDPN, TNFSF13B, MAGT1, IL33, RBM45, PEBP1, LTA, MST1, LTBR, ALPP, APOA2, CA2, CALCB, CD47, CDKN1A, CTLA4, DOCK3, ENO1, GSTT1, HLA-DOA, HP, HSPE1, IAPP, IFNA1, IFNA13, IL10, KCNA3, ALPI, HT

Drugs

Humanised Fc-engineered monoclonal antibody against CD19

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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 which affects elderly males, involves other organs and has increased immunoglobin G4 (IgG4) levels and type 2 which affects both sexes equally but presents at a younger age and has no other organ involvement or increased IgG4 levels.