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11766001: Gerlier's disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
20315018 Gerlier's disease en Synonym Active Entire term case sensitive SNOMED CT core module
20316017 Paralyzing vertigo en Synonym Active Entire term case insensitive SNOMED CT core module
20317014 Endemic paralytic vertigo en Synonym Active Entire term case insensitive SNOMED CT core module
691822014 Gerlier's disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2838975010 Gerlier disease en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Gerlier's disease Is a Labyrinthine disorder true Inferred relationship Existential restriction modifier
Gerlier's disease Is a Disorders of the vestibular system and vertiginous syndromes false Inferred relationship Existential restriction modifier
Gerlier's disease Finding site Labyrinth structure true Inferred relationship Existential restriction modifier 1
Gerlier's disease Has definitional manifestation Dizziness false Inferred relationship Existential restriction modifier
Gerlier's disease Has definitional manifestation Vertigo false Inferred relationship Existential restriction modifier
Gerlier's disease Has definitional manifestation Vertigo false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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