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

713060000: Sporadic Creutzfeldt-Jakob disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3287808015 Sporadic Creutzfeldt-Jakob disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3287830019 Sporadic Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303328013 Sporadic Jakob-Creutzfeldt disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
888781000172117 maladie de Creutzfeldt-Jakob sporadique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
983221000172114 MCJ (maladie de Creutzfeldt-Jakob) sporadique fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2299531000195115 Sporadische Creutzfeldt-Jakob-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sporadic Creutzfeldt-Jakob disease (disorder) Is a Creutzfeldt-Jakob disease true Inferred relationship Some
Sporadic Creutzfeldt-Jakob disease (disorder) Is a syndrome cérébral non spécifique false Inferred relationship Some
Sporadic Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration false Inferred relationship Some 2
Sporadic Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Creutzfeldt-Jakob agent false Inferred relationship Some 2
Sporadic Creutzfeldt-Jakob disease (disorder) Finding site Brain tissue structure false Inferred relationship Some 2
Sporadic Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) false Inferred relationship Some 2
Sporadic Creutzfeldt-Jakob disease (disorder) Associated morphology dégénérescence false Inferred relationship Some 3
Sporadic Creutzfeldt-Jakob disease (disorder) Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Some 3
Sporadic Creutzfeldt-Jakob disease (disorder) Finding site Brain structure true Inferred relationship Some 1
Sporadic Creutzfeldt-Jakob disease (disorder) Associated morphology Spongy degeneration true Inferred relationship Some 1
Sporadic Creutzfeldt-Jakob disease (disorder) Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Some 1
Sporadic Creutzfeldt-Jakob disease (disorder) Causative agent (attribute) Creutzfeldt-Jakob agent true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Classical sporadic Creutzfeldt-Jakob disease Is a True Sporadic Creutzfeldt-Jakob disease (disorder) Inferred relationship Some
Sporadic fatal insomnia Is a True Sporadic Creutzfeldt-Jakob disease (disorder) Inferred relationship Some
Dementia due to sporadic Creutzfeldt-Jakob disease (disorder) Due to True Sporadic Creutzfeldt-Jakob disease (disorder) Inferred relationship Some 3

This concept is not in any reference sets

Back to Start