715807002: Familial Creutzfeldt-Jakob (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\constatation à propos l'encéphale\Disorder of brain (disorder)\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Infectious disease of central nervous system\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)

\constatation à propos d'une région de la tête et du cou\Head finding (finding)\...

\constatation à propos l'encéphale\Disorder of brain (disorder)\...

\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)

\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)

\affection de la tête\trouble infectieux de la tête\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\affection de la tête\Disorder of brain (disorder)\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\affection de la tête\Disorder of brain (disorder)\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection dégénérative\maladie dégénérative du système nerveux central\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Infectious disease of nervous system\Infectious disease of central nervous system\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Infectious disease of central nervous system\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\maladie dégénérative du système nerveux central\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection de la tête\trouble infectieux de la tête\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection de la tête\Disorder of brain (disorder)\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\affection de la tête\Disorder of brain (disorder)\Degenerative brain disorder\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\maladie infectieuse\trouble infectieux de la tête\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\Familial Creutzfeldt-Jakob (disorder)
\Disease\maladie infectieuse\Infectious disease of nervous system\Infectious disease of central nervous system\maladie infectieuse de l'encéphale\maladie à prion\maladie de Creutzfeldt-Jakob\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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial Creutzfeldt-Jakob (disorder)	est un(e) (attribut)	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Some
Familial Creutzfeldt-Jakob (disorder)	est un(e) (attribut)	maladie de Creutzfeldt-Jakob	true	Inferred relationship	Some
Familial Creutzfeldt-Jakob (disorder)	est un(e) (attribut)	Hereditary disorder of nervous system	false	Inferred relationship	Some
Familial Creutzfeldt-Jakob (disorder)	morphologie associée (attribut)	Spongy degeneration	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob (disorder)	Causative agent	Creutzfeldt-Jakob agent	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob (disorder)	localisation d'une constatation (attribut)	structure du tissu encéphalique	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob (disorder)	Pathological process (attribute)	Infectious process (qualifier value)	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob (disorder)	est un(e) (attribut)	Autosomal dominant hereditary disorder	true	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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