Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302234010 | Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302235011 | Primary biliary cirrhosis co-occurrent with systemic scleroderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302236012 | Reynolds syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400852010 | Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400853017 | Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302234010 | Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302234010 | Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302235011 | Primary biliary cirrhosis co-occurrent with systemic scleroderma | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3302235011 | Primary biliary cirrhosis co-occurrent with systemic scleroderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3302236012 | Reynolds syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302474019 | An autoimmune disorder characterized by the association of primary biliary cirrhosis with limited cutaneous systemic sclerosis. Onset occurs between 30-65 years. Occurs sporadically, but rare familial cases with an unknown inheritance pattern have been observed. There is no cure and management is mainly supportive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3302475018 | An autoimmune disorder characterised by the association of primary biliary cirrhosis with limited cutaneous systemic sclerosis. Onset occurs between 30-65 years. Occurs sporadically, but rare familial cases with an unknown inheritance pattern have been observed. There is no cure and management is mainly supportive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400852010 | Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400853017 | Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3414791001000112 | Reynolds-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
213951000172111 | syndrome de Reynolds | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
213951000172111 | syndrome de Reynolds | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3414791001000112 | Reynolds-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Is a | Primary biliary cholangitis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Is a | Systemic sclerosis | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Autoimmune process | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Fibrosis (morphologic abnormality) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 4 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Bile duct structure | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 4 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Fibrosis (morphologic abnormality) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Fibrosis (morphologic abnormality) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 6 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic biliary tree (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 6 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Nodular regeneration | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Liver structure (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 4 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Liver structure (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Liver structure (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Chronic fibrosis | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Nodular regeneration | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Fibrosis (morphologic abnormality) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Is a | Progressive systemic sclerosis (disorder) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Connective tissue structure (body structure) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Is a | Systemic sclerosis with limited cutaneous involvement | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic biliary tree (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic biliary tree (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic biliary tree (body structure) | false | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Pathological process (attribute) | Hypersensitivity process (qualifier value) | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 6 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic bile duct | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 5 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic bile duct | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Chronic fibrosis | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Finding site | Structure of intrahepatic bile duct | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). | Associated morphology | Nodular regeneration | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)