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716196007: Isolated polycystic liver disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3305052010 Isolated polycystic liver disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305053017 Isolated polycystic liver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401259019 Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401260012 Isolated polycystic liver disease (PCLD) is a genetic disorder characterised by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3305052010 Isolated polycystic liver disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3305052010 Isolated polycystic liver disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305053017 Isolated polycystic liver disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3305053017 Isolated polycystic liver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3305054011 A genetic disorder with characteristics of the appearance of numerous cysts spread throughout the liver. Women are predominantly affected and have a larger number of cysts than affected males. Cysts are undetectable early in life and usually appear after the age of 40 years. Their number and size increases with age. Symptoms depend on the mass (compression effect) some patients are asymptomatic. Liver function is usually normal. There is no portal hypertension. Extrahepatic manifestations are very rare and may include intracranial aneurysms (usually small sized and at a low risk of rupture) and mitral leaflet abnormalities. Liver cysts result from overgrowth of biliary epithelium or from dilatation of peribiliary glands. Some cases occur sporadically, but most are inherited as an autosomal dominant trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401259019 Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401260012 Isolated polycystic liver disease (PCLD) is a genetic disorder characterised by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3411121001000111 Lebererkrankheit, isolierte polyzystische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962361000172118 polykystose hépatique isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968531000172119 ADPCLD - autosomal dominant polycystic liver disease fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
962361000172118 polykystose hépatique isolée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
968531000172119 ADPCLD - autosomal dominant polycystic liver disease fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3411121001000111 Lebererkrankheit, isolierte polyzystische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Is a Liver cyst true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Associated morphology Polycystic change true Inferred relationship Existential restriction modifier (core metadata concept) 1
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Finding site Liver structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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