Hereditary chronic pancreatitis (HCP), a rare inherited form of pancreatitis is defined as recurrent acute pancreatitis and/or chronic pancreatitis in two first-degree relatives or 3 or more second-degree relatives in 2 or more generations, for which no predisposing factors are identified. HCP is characterized by irreversible damage to both exocrine and endocrine components of the pancreas. [ Orphanet:676 ]
Synonyms: hereditary chronic pancreatitis hereditary pancreatitis
Term information
- Orphanet:676 (OMIM:167800)
- MESH:C537262 (MONDO:equivalentTo)
- SCTID:68072000 (MONDO:equivalentTo)
- OMIM:167800 (Orphanet:676/e)
- GARD:6632 (Orphanet:676)
- ICD9:577.8 (MONDO:relatedTo)
- NCIT:C95436 (MONDO:equivalentTo)
gard_rare, ordo_disease, rare, predisposition, nord_rare, orphanet_rare, clingen
http://www.orpha.net/ORDO/Orphanet_676
http://identifiers.org/snomedct/68072000
http://identifiers.org/mesh/C537262
https://omim.org/entry/167800
http://purl.obolibrary.org/obo/NCIT_C95436
pancreatitis, calcific, included
autosomal dominant hereditary pancreatitis
Hp
pancreatitis, chronic pancreatitis, chronic, susceptibility to, included
pancreatitis, chronic, susceptibility to
pancreatitis, calcific
pancreatitis, chronic
familial pancreatitis
PCTT
pancreatitis, chronic, protection against, included
pancreatitis, hereditary
HPC
pancreatitis, chronic, protection against
https://search.clinicalgenome.org/kb/conditions/MONDO:0008185
https://rarediseases.info.nih.gov/diseases/6632/hereditary-pancreatitis