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11766001: Gerlier's disease (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
20315018 Gerlier's disease en Synonym Active Case sensitive SNOMED CT core
20316017 Paralyzing vertigo en Synonym Active Case insensitive SNOMED CT core
20317014 Endemic paralytic vertigo en Synonym Active Case insensitive SNOMED CT core
2838975010 Gerlier disease en Synonym Active Case sensitive SNOMED CT core
691822014 Gerlier's disease (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
Gerlier's disease Is a Labyrinthine disorder true Inferred relationship Some
Gerlier's disease Is a Disorders of the vestibular system and vertiginous syndromes false Inferred relationship Some
Gerlier's disease Has definitional manifestation Vertigo false Inferred relationship Some
Gerlier's disease Has definitional manifestation Vertigo false Inferred relationship Some
Gerlier's disease Finding site Labyrinth structure true Inferred relationship Some 1
Gerlier's disease Has definitional manifestation Dizziness false Inferred relationship Some

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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