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64770007: Nodular regeneration (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
107652016 Nodular regeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
804199014 Nodular regeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nodular regeneration Is a Regeneration true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Nutritional cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 1
Unilobular portal cirrhosis Associated morphology False Nodular regeneration Inferred relationship Some 1
Florid cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 1
Hepatic fibrosis with hepatic sclerosis Associated morphology False Nodular regeneration Inferred relationship Some 1
Cirrhosis of liver not due to alcohol Associated morphology False Nodular regeneration Inferred relationship Some 1
Alcoholic cirrhosis (disorder) Associated morphology False Nodular regeneration Inferred relationship Some 1
Cryptogenic cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 1
Portal and splenic vein sclerosis Associated morphology False Nodular regeneration Inferred relationship Some 1
Cruveilhier-Baumgarten syndrome Associated morphology True Nodular regeneration Inferred relationship Some 1
cirrhose cardiotuberculeuse Associated morphology False Nodular regeneration Inferred relationship Some 1
Parasitic cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 1
Infectious cirrhosis Associated morphology False Nodular regeneration Inferred relationship Some 1
Juvenile portal cirrhosis Associated morphology False Nodular regeneration Inferred relationship Some 1
Syphilitic portal cirrhosis Associated morphology False Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver due to chronic hepatitis C Associated morphology False Nodular regeneration Inferred relationship Some 2
Severe autosomal recessive intrahepatic cholestasis described in aboriginal children from northwestern Quebec. First manifestation as neonatal jaundice, progresses to periportal fibrosis and cirrhosis. Associated morphology True Nodular regeneration Inferred relationship Some 2
Syphilitic cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver due to hepatitis B Associated morphology True Nodular regeneration Inferred relationship Some 1
Cirrhosis of liver due to hepatitis B Associated morphology False Nodular regeneration Inferred relationship Some 2
Infectious cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Syphilitic portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Nodular regenerative hyperplasia Is a True Nodular regeneration Inferred relationship Some
Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). Associated morphology False Nodular regeneration Inferred relationship Some 5
Decompensated cirrhosis of liver (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 1
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. Associated morphology False Nodular regeneration Inferred relationship Some 4
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. Associated morphology False Nodular regeneration Inferred relationship Some 4
Cirrhosis of liver caused by methotrexate (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver caused by amiodarone (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver caused by methyldopa (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) Associated morphology False Nodular regeneration Inferred relationship Some 4
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 1
Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). Associated morphology False Nodular regeneration Inferred relationship Some 1
Cirrhosis of liver due to chronic hepatitis C Associated morphology True Nodular regeneration Inferred relationship Some 1
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. Associated morphology True Nodular regeneration Inferred relationship Some 1
Cirrhotic cardiomyopathy is the term used to describe a constellation of features indicative of abnormal heart structure and function in patients with cirrhosis. These include systolic and diastolic dysfunction, electrophysiological changes, and macroscopic and microscopic structural changes. Associated morphology True Nodular regeneration Inferred relationship Some 2
Primary biliary cholangitis Associated morphology False Nodular regeneration Inferred relationship Some 2
Clonorchiasis with biliary cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 1
Micronodular regeneration Is a True Nodular regeneration Inferred relationship Some
Macronodular regeneration Is a True Nodular regeneration Inferred relationship Some
Toxic portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Bacterial portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis of liver due to and following cardiac procedure (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 2
Liver cirrhosis due to classical cystic fibrosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Juvenile portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Unilobular portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Cirrhosis resulting from accumulation of iron in the liver. Associated morphology True Nodular regeneration Inferred relationship Some 2
Pigmentary portal cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Drug-induced cirrhosis of liver (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 2
Indian childhood cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Biliary cirrhosis of children Associated morphology True Nodular regeneration Inferred relationship Some 3
Toxic cirrhosis Associated morphology True Nodular regeneration Inferred relationship Some 2
Alcoholic cirrhosis (disorder) Associated morphology True Nodular regeneration Inferred relationship Some 3
Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). Associated morphology True Nodular regeneration Inferred relationship Some 2

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