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722949001: Familial Ménière disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334418010 Familial Ménière disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334419019 Familial Ménière disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334418010 Familial Ménière disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334419019 Familial Ménière disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6177891000241118 maladie de Ménière familiale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6177891000241118 maladie de Ménière familiale fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial Ménière disease (disorder) Is a Ménière's disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial Ménière disease (disorder) Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial Ménière disease (disorder) Finding site Labyrinth structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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