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715807002: Familial Creutzfeldt-Jakob (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3303774010 Familial Creutzfeldt-Jakob (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303775011 Familial Creutzfeldt-Jakob en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303776012 fCJD (Familial Creutzfeldt-Jakob disease) en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307459013 Inherited Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307460015 Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307461016 Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterised by typical CJD features (rapidly progressive dementia, personality/behavioural changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303774010 Familial Creutzfeldt-Jakob (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303775011 Familial Creutzfeldt-Jakob en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303776012 fCJD (Familial Creutzfeldt-Jakob disease) en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307459013 Inherited Creutzfeldt-Jakob disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307460015 Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307461016 Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterised by typical CJD features (rapidly progressive dementia, personality/behavioural changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3435201001000117 Creutzfeldt-Jakob-Krankheit, hereditäre de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6177821000241116 MCJ (maladie de Creutzfeldt-Jakob) familiale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6177831000241119 maladie de Creutzfeldt-Jakob familiale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6177821000241116 MCJ (maladie de Creutzfeldt-Jakob) familiale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6177831000241119 maladie de Creutzfeldt-Jakob familiale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435201001000117 Creutzfeldt-Jakob-Krankheit, hereditäre 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
Familial Creutzfeldt-Jakob (disorder) Is a Jakob-Creutzfeldt disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial Creutzfeldt-Jakob (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial Creutzfeldt-Jakob (disorder) Associated morphology Spongy degeneration (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial Creutzfeldt-Jakob (disorder) Causative agent (attribute) Creutzfeldt-Jakob agent true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial Creutzfeldt-Jakob (disorder) Finding site Brain tissue structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial Creutzfeldt-Jakob (disorder) Pathological process (attribute) Infectious process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial Creutzfeldt-Jakob (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Familial Creutzfeldt-Jakob (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Familial Creutzfeldt-Jakob (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Dementia due to familial Creutzfeldt-Jakob disease Due to True Familial Creutzfeldt-Jakob (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3

This concept is not in any reference sets

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