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716196007: Isolated polycystic liver disease (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3305053017 Isolated polycystic liver disease en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated polycystic liver disease Is a Liver cyst true Inferred relationship Some
Isolated polycystic liver disease Is a Digestive system hereditary disorder true Inferred relationship Some
Isolated polycystic liver disease Associated morphology Polycystic change true Inferred relationship Some 1
Isolated polycystic liver disease Finding site Liver structure true 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

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