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autoimmune pancreatitis

Go to external page http://purl.obolibrary.org/obo/MONDO_0015175

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. [ Orphanet:103919 ]

Synonyms: AIP

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:750633 (MONDO:equivalentTo)
  • Orphanet:103919 (MONDO:equivalentTo)
  • NANDO:2200943 (https://orcid.org/0000-0003-0011-764X)
  • DOID:0040091 (MONDO:equivalentTo)
  • icd11.foundation:2057951941 (Orphanet:103919)
  • GARD:10911 (MONDO:GARD)
  • MedDRA:10069002 (Orphanet:103919/e)
  • NANDO:1200925 (https://orcid.org/0000-0003-0011-764X)
  • MESH:D000081012 (https://orcid.org/0000-0003-1967-3726)
  • UMLS:C2609129 (MONDO:equivalentTo)
  • SCTID:448542008 (MONDO:equivalentTo)
Subsets

gard_rare, otar, rare, nord_rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5537

closeMatch

http://identifiers.org/meddra/10069002

exactMatch

http://purl.obolibrary.org/obo/DOID_0040091

http://linkedlifedata.com/resource/umls/id/C2609129

http://identifiers.org/snomedct/448542008

http://identifiers.org/mesh/D000081012

http://www.orpha.net/ORDO/Orphanet_103919

http://identifiers.org/medgen/750633

has related synonym

lymphoplasmocytic sclerosing pancreatitis

id

MONDO:0015175