MeSH Browser

MeSH Supplementary: Hereditary pancreatitis
Unique ID: C537262
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537262
Entry Term(s): Autosomal Dominant Hereditary Pancreatitis; Familial Pancreatitis; Hereditary Chronic Pancreatitis; Pancreatitis, Hereditary
Registry Numbers: 0
Heading Mapped to: *Pancreatitis, Chronic
Frequency: 72
Note: Hereditary autosomal dominant forms of chronic pancreatitis that are associated with mutations in the CTRC, SPINK1, and PRSS1 genes. Mutations in the CFTR gene have been identified in cases of idiopathic pancreatitis. OMIM: 167800
Date of Entry: 2010/08/25
Revision Date: 2015/09/26

Concept UI: M0531723
Registry Numbers: 0
Terms: Hereditary pancreatitis Preferred Term
Term UI T741987
Date02/24/2009
LexicalTag NON
ThesaurusID; Pancreatitis, Hereditary
Term UI T800761
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Familial Pancreatitis
Term UI T841633
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Hereditary Chronic Pancreatitis
Term UI T841634
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Hereditary pancreatitis MeSH Supplementary Concept Data 2025