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702426001: GRN-related frontotemporal dementia (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2995549015 Hereditary dysphasic disinhibition dementia en Synonym Active Case insensitive SNOMED CT core
2995667018 Frontotemporal lobar degeneration en Synonym Active Case insensitive SNOMED CT core
2995747016 GRN-related frontotemporal dementia en Synonym Active Case sensitive SNOMED CT core
2995756012 GRN-related frontotemporal dementia (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
GRN-related frontotemporal dementia Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
GRN-related frontotemporal dementia Associated morphology Degenerative abnormality true Inferred relationship Some 1
GRN-related frontotemporal dementia Is a Autosomal dominant hereditary disorder true Inferred relationship Some
GRN-related frontotemporal dementia Is a Degenerative brain disorder true Inferred relationship Some
GRN-related frontotemporal dementia Is a Hereditary disorder of nervous system false Inferred relationship Some
GRN-related frontotemporal dementia Associated morphology Degeneration false Inferred relationship Some 1
GRN-related frontotemporal dementia Finding site Brain tissue structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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