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1260354005: Frontotemporal dementia due to C9orf72 mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5160218010 Frontotemporal dementia due to C9orf72 mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5160219019 Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5168677018 Frontotemporal dementia due to C9orf72 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Frontotemporal dementia due to C9orf72 mutation (disorder) Is a Cerebral degeneration associated with another disorder (disorder) true Inferred relationship Some
Frontotemporal dementia due to C9orf72 mutation (disorder) Is a Frontotemporal dementia true Inferred relationship Some
Frontotemporal dementia due to C9orf72 mutation (disorder) Due to Anomaly of chromosome pair 9 true Inferred relationship Some 3
Frontotemporal dementia due to C9orf72 mutation (disorder) Finding site Temporal lobe structure true Inferred relationship Some 1
Frontotemporal dementia due to C9orf72 mutation (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Frontotemporal dementia due to C9orf72 mutation (disorder) Finding site Frontal lobe structure true Inferred relationship Some 2
Frontotemporal dementia due to C9orf72 mutation (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2
Frontotemporal dementia due to C9orf72 mutation (disorder) Is a Dementia due to chromosomal anomaly (disorder) true Inferred relationship Some
Frontotemporal dementia due to C9orf72 mutation (disorder) Interprets Cognitive functions true Inferred relationship Some 4
Frontotemporal dementia due to C9orf72 mutation (disorder) Has interpretation Impaired true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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