FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

84676004: Prion (organism)

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
140386019 Prion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
140388018 Proteinaceous infectious particle en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
140389014 Prion protein en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
826569019 Prion (organism) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
20481000077113 prion fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
617181000172113 Prion fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3087621001000117 Prion de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

11 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prion Is a Infectious agent false Inferred relationship Some
Prion Is a micro-organisme false Inferred relationship Some
Prion Is a agent infectieux opportuniste false Inferred relationship Some
Prion Is a Infectious agent false Inferred relationship Some
Prion Is a micro-organisme false Inferred relationship Some
Prion Is a Organism (organism) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Spongiform encephalopathy agent Is a True Prion Inferred relationship Some
Spongiform encephalopathy Causative agent (attribute) False Prion Inferred relationship Some
Prion disease Causative agent (attribute) False Prion Inferred relationship Some
Transmissible mink encephalopathy Causative agent (attribute) False Prion Inferred relationship Some
Fatal familial insomnia Causative agent (attribute) False Prion Inferred relationship Some
Progressive subcortical gliosis Causative agent (attribute) False Prion Inferred relationship Some
Slow viral central nervous system infection Causative agent (attribute) False Prion Inferred relationship Some
Cerebral degeneration due to Creutzfeldt-Jakob disease Causative agent (attribute) False Prion Inferred relationship Some
Other slow virus central nervous system infections Causative agent (attribute) False Prion Inferred relationship Some
Slow virus central nervous system infection NOS Causative agent (attribute) False Prion Inferred relationship Some
[X]Other slow virus infections of central nervous system Causative agent (attribute) False Prion Inferred relationship Some
[X]Slow virus infection of central nervous system, unspecified Causative agent (attribute) False Prion Inferred relationship Some
[X]Dementia in Creutzfeldt-Jakob disease Causative agent (attribute) False Prion Inferred relationship Some
AIDS with slow virus infection Causative agent (attribute) False Prion Inferred relationship Some
maladie à prion associée au SIDA Causative agent (attribute) False Prion Inferred relationship Some
Gerstmann-Straussler-Scheinker syndrome Causative agent (attribute) False Prion Inferred relationship Some 2
Creutzfeldt-Jakob disease Causative agent (attribute) False Prion Inferred relationship Some 3
Prion disease Causative agent (attribute) False Prion Inferred relationship Some 3
Spongiform encephalopathy Causative agent (attribute) False Prion Inferred relationship Some 2
Kuru Causative agent (attribute) False Prion Inferred relationship Some 2
Fatal familial insomnia Causative agent (attribute) False Prion Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) False Prion Inferred relationship Some 2
Progressive subcortical gliosis Causative agent (attribute) False Prion Inferred relationship Some 3
Familial Alzheimer-like prion disease is an exceedingly rare form of prion disease characterized by the neuropathological features of Alzheimer disease including memory impairment and depression, related to abnormal prion protein (PrP) caused by a gene mutation in PRNP. Patients present with a prolonged, atypical course (absence of myoclonus or ataxia) unlike other forms of prion disease with severe neurofibrillary tangle pathology and high levels of cerebral amyloidosis. Causative agent (attribute) True Prion Inferred relationship Some 1
A rare, autosomal dominant neurological disorder due to truncation mutations of the prion protein gene PRNP (20p13) leading to deposition of prion protein amyloid. Onset is usually in the fourth decade of life and reported clinical manifestations include diarrhea, nausea, autonomic failure (areflexia, weakness), neurogenic bladder and urinary infections. Causative agent (attribute) True Prion Inferred relationship Some 2
Spongiform encephalopathy Causative agent (attribute) True Prion Inferred relationship Some 1
Progressive subcortical gliosis Causative agent (attribute) True Prion Inferred relationship Some 1
Prion disease Causative agent (attribute) True Prion Inferred relationship Some 1

This concept is not in any reference sets

Back to Start