717232005: Caroli disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Liver finding\Liver disease\Congenital anomaly of liver\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease

\Digestive system finding\Finding of biliary tract\Disorder of biliary tract\Congenital anomaly of biliary tract\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Finding of biliary tract\Disorder of biliary tract\Cholangiectasis\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Finding of biliary tract\Disorder of biliary tract\Disorder of bile duct\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Liver finding\Liver disease\Congenital anomaly of liver\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Liver disease\Congenital anomaly of liver\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Congenital anomaly of digestive organ\Congenital abnormality of liver and/or biliary tract\Congenital anomaly of biliary tract\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Congenital anomaly of digestive organ\Congenital abnormality of liver and/or biliary tract\Congenital anomaly of liver\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of biliary tract\Congenital anomaly of biliary tract\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of biliary tract\Cholangiectasis\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of biliary tract\Disorder of bile duct\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Congenital anomaly of digestive system\Congenital anomaly of digestive organ\Congenital abnormality of liver and/or biliary tract\Congenital anomaly of biliary tract\Congenital anomaly of bile ducts\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease
\Digestive system finding\Disorder of digestive system\Congenital anomaly of digestive system\Congenital anomaly of digestive organ\Congenital abnormality of liver and/or biliary tract\Congenital anomaly of liver\Congenital dilatation of lobar intrahepatic bile duct\Caroli disease

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3308765010 Caroli disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core

3308766011 Caroli disease en Synonym Active Case sensitive SNOMED CT core

3308767019 A rare congenital disorder characterized by multifocal, segmental dilatation of the large intrahepatic bile ducts. It may present at any age and predominantly affects females. Less than 250 cases have been described worldwide. Caroli disease is characterized by bile ductal ectasia without other apparent hepatic abnormalities. It presents with recurrent bacterial cholangitis, biliary stones causing biliary pain or episodes of pancreatitis. The more common variant of this disease, named Caroli syndrome, is characterized by dilatations of the large bile duct associated with congenital hepatic fibrosis. The etiology of Caroli disease is unknown and its occurrence is sporadic, whereas Caroli syndrome is generally inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core

3308768012 A rare congenital disorder characterised by multifocal, segmental dilatation of the large intrahepatic bile ducts. It may present at any age and predominantly affects females. Less than 250 cases have been described worldwide. Caroli disease is characterised by bile ductal ectasia without other apparent hepatic abnormalities. It presents with recurrent bacterial cholangitis, biliary stones causing biliary pain or episodes of pancreatitis. The more common variant of this disease, named Caroli syndrome, is characterised by dilatations of the large bile duct associated with congenital hepatic fibrosis. The aetiology of Caroli disease is unknown and its occurrence is sporadic, whereas Caroli syndrome is generally inherited in an autosomal recessive manner. en Definition Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Caroli disease	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Caroli disease	Associated morphology	Dilatation	true	Inferred relationship	Some	1
Caroli disease	Finding site	Structure of wall of intrahepatic biliary tract	true	Inferred relationship	Some	1
Caroli disease	Is a	Congenital dilatation of lobar intrahepatic bile duct	true	Inferred relationship	Some
Caroli disease	Associated morphology	Congenital dilatation	false	Inferred relationship	Some	1
Caroli disease	Occurrence	Congenital	true	Inferred relationship	Some	1
Caroli disease	Finding site	Intrahepatic biliary tract structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3308765010	Caroli disease (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
3308766011	Caroli disease	en	Synonym	Active	Case sensitive	SNOMED CT core
3308767019	A rare congenital disorder characterized by multifocal, segmental dilatation of the large intrahepatic bile ducts. It may present at any age and predominantly affects females. Less than 250 cases have been described worldwide. Caroli disease is characterized by bile ductal ectasia without other apparent hepatic abnormalities. It presents with recurrent bacterial cholangitis, biliary stones causing biliary pain or episodes of pancreatitis. The more common variant of this disease, named Caroli syndrome, is characterized by dilatations of the large bile duct associated with congenital hepatic fibrosis. The etiology of Caroli disease is unknown and its occurrence is sporadic, whereas Caroli syndrome is generally inherited in an autosomal recessive manner.	en	Definition	Active	Case sensitive	SNOMED CT core
3308768012	A rare congenital disorder characterised by multifocal, segmental dilatation of the large intrahepatic bile ducts. It may present at any age and predominantly affects females. Less than 250 cases have been described worldwide. Caroli disease is characterised by bile ductal ectasia without other apparent hepatic abnormalities. It presents with recurrent bacterial cholangitis, biliary stones causing biliary pain or episodes of pancreatitis. The more common variant of this disease, named Caroli syndrome, is characterised by dilatations of the large bile duct associated with congenital hepatic fibrosis. The aetiology of Caroli disease is unknown and its occurrence is sporadic, whereas Caroli syndrome is generally inherited in an autosomal recessive manner.	en	Definition	Active	Case sensitive	SNOMED CT core