MeSH Browser

MeSH Heading: Choledochal Cyst
Tree Number(s): C04.182.198; C06.130.120.127; C06.198.184; C16.131.314.184
Unique ID: D015529
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D015529
Annotation: non-neoplastic
Scope Note: A congenital anatomic malformation of a bile duct, including cystic dilatation of the extrahepatic bile duct or the large intrahepatic bile duct. Classification is based on the site and type of dilatation. Type I is most common.
Entry Term(s): Bile Duct Cysts; Choledochal Cyst, Diverticulum; Choledochal Cyst, Type I; Choledochal Cyst, Type II; Choledochal Cyst, Type III; Choledochal Cyst, Type IV; Choledochal Cyst, Type V; Choledochal Diverticulum; Choledochocele; Common Bile Duct Cyst; Congenital Biliary Dilatation; Congenital Choledochal Cyst; Cyst, Common Bile Duct; Cysts, Common Bile Duct; Intrahepatic Choledochal Cyst; Multiple Choledochal Cysts
NLM Classification #: WI 753
Previous Indexing: Biliary Tract Diseases (1972-1979); Common Bile Duct (1966-1979); Common Bile Duct Diseases (1980-1989); Cysts (1966-1989)
Public MeSH Note: 1990
History Note: 1990
Date Established: 1990/01/01
Date of Entry: 1989/04/07
Revision Date: 2019/02/22

Allowable Qualifiers: blood (BL)

blood supply (BS)

cerebrospinal fluid (CF)

chemically induced (CI)

chemistry (CH)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

ultrastructure (UL)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0023892
Scope Note: A congenital anatomic malformation of a bile duct, including cystic dilatation of the extrahepatic bile duct or the large intrahepatic bile duct. Classification is based on the site and type of dilatation. Type I is most common.
Terms: Choledochal Cyst Preferred Term
Term UI T046033
Date01/01/1999
LexicalTag NON
ThesaurusID; Choledochocele
Term UI T526151
Date11/15/2002
LexicalTag NON
ThesaurusID; Congenital Choledochal Cyst
Term UI T750931
Date05/12/2009
LexicalTag NON
ThesaurusID; Bile Duct Cysts
Term UI T812528
Date11/15/2011
LexicalTag NON
ThesaurusID

Concept UI: M0023893
Scope Note: Characterized by the fusiform or saccular dilatation of the COMMON BILE DUCT.
Terms: Choledochal Cyst, Type I Preferred Term
Term UI T521038
Date10/02/2002
LexicalTag NON
ThesaurusID NLM (2004); Cyst, Common Bile Duct
Term UI T046034
Date02/28/1989
LexicalTag NON
ThesaurusID NLM (1990); Cysts, Common Bile Duct
Term UI T046035
Date02/28/1989
LexicalTag NON
ThesaurusID NLM (1990); Common Bile Duct Cyst
Term UI T046036
Date02/28/1989
LexicalTag NON
ThesaurusID NLM (1990)

Choledochal Cyst MeSH Descriptor Data 2024