FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

715401008: Primary biliary cirrhosis co-occurrent with systemic scleroderma (disorder)


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


0 descendants.

Expanded Value Set


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)

Back to Start