702393003: Frontotemporal dementia with gene located on 3p11 (disorder)

SNOMED CT Concept\Clinical finding\...

\Central nervous system finding\Finding of brain\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Central nervous system finding\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11

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

\Finding of brain\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11

\Finding of head region\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11

\Disorder of head\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Frontotemporal dementia with gene located on 3p11
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Disease\Degenerative disorder\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Hereditary degenerative disease of central nervous system\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Degenerative disease of the central nervous system\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11
\Disease\Disorder of head\Disorder of brain\Degenerative brain disorder\Cerebral degeneration\Frontotemporal degeneration\Frontotemporal dementia\Frontotemporal dementia with gene located on 3p11

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2995032019 Frontotemporal dementia with gene located on 3p11 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2995083019 Frontotemporal dementia with gene located on 3p11 en Synonym Active Entire term case insensitive SNOMED CT core module

2995149012 Chromosome 3-linked frontotemporal dementia en Synonym Active Entire term case insensitive SNOMED CT core module

2995366019 CHMP2B-related frontotemporal dementia en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Frontotemporal dementia with gene located on 3p11	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Frontotemporal dementia with gene located on 3p11	Is a	Frontotemporal dementia	true	Inferred relationship	Existential restriction modifier
Frontotemporal dementia with gene located on 3p11	Is a	Hereditary disorder of nervous system	false	Inferred relationship	Existential restriction modifier
Frontotemporal dementia with gene located on 3p11	Associated morphology	Degeneration	false	Inferred relationship	Existential restriction modifier	1
Frontotemporal dementia with gene located on 3p11	Finding site	Temporal lobe structure	false	Inferred relationship	Existential restriction modifier	1
Frontotemporal dementia with gene located on 3p11	Finding site	Frontal lobe structure	true	Inferred relationship	Existential restriction modifier	1
Frontotemporal dementia with gene located on 3p11	Is a	Hereditary degenerative disease of central nervous system	true	Inferred relationship	Existential restriction modifier
Frontotemporal dementia with gene located on 3p11	Finding site	Temporal lobe structure	true	Inferred relationship	Existential restriction modifier	2
Frontotemporal dementia with gene located on 3p11	Associated morphology	Degenerative abnormality	true	Inferred relationship	Existential restriction modifier	1
Frontotemporal dementia with gene located on 3p11	Associated morphology	Degenerative abnormality	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2995032019	Frontotemporal dementia with gene located on 3p11 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2995083019	Frontotemporal dementia with gene located on 3p11	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2995149012	Chromosome 3-linked frontotemporal dementia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2995366019	CHMP2B-related frontotemporal dementia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module