715807002: Familial Creutzfeldt-Jakob (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Encephalopathy\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Central nervous system finding\Finding of brain\Encephalopathy\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Central nervous system finding\Disorder of the central nervous system\Infectious disease of central nervous system\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob

\Finding of head and neck region\Head finding\...

\Finding of brain\Encephalopathy\...

\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob

\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob

\Disorder of head\Infective disorder of head\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disorder of head\Encephalopathy\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disorder of head\Encephalopathy\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial Creutzfeldt-Jakob
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Infectious disease of nervous system\Infectious disease of central nervous system\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Infectious disease of central nervous system\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Familial Creutzfeldt-Jakob
\Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of head\Infective disorder of head\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of head\Encephalopathy\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Disorder of head\Encephalopathy\Degenerative brain disorder\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Infection\Infective disorder of head\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob
\Disease\Infection\Infectious disease of nervous system\Infectious disease of central nervous system\Infectious disease of brain\Prion disease\Jakob-Creutzfeldt disease\Familial Creutzfeldt-Jakob

Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core

3303775011 Familial Creutzfeldt-Jakob en Synonym Active Initial character case insensitive SNOMED CT core

3303776012 fCJD (Familial Creutzfeldt-Jakob disease) en Synonym Active Case sensitive SNOMED CT core

3307459013 Inherited Creutzfeldt-Jakob disease en Synonym Active Initial character case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial Creutzfeldt-Jakob	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Some
Familial Creutzfeldt-Jakob	Is a	Jakob-Creutzfeldt disease	true	Inferred relationship	Some
Familial Creutzfeldt-Jakob	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Some
Familial Creutzfeldt-Jakob	Associated morphology	Spongy degeneration	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob	Causative agent	Creutzfeldt-Jakob agent	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob	Finding site	Brain tissue structure	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob	Pathological process	Infectious process	true	Inferred relationship	Some	1
Familial Creutzfeldt-Jakob	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Dementia due to familial Creutzfeldt-Jakob disease	Due to	True	Familial Creutzfeldt-Jakob	Inferred relationship	Some	3

Reference Sets

Disease caused by microorganism or bacterial toxin reference set

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3303774010	Familial Creutzfeldt-Jakob (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3303775011	Familial Creutzfeldt-Jakob	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3303776012	fCJD (Familial Creutzfeldt-Jakob disease)	en	Synonym	Active	Case sensitive	SNOMED CT core
3307459013	Inherited Creutzfeldt-Jakob disease	en	Synonym	Active	Initial character case insensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core