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471885006: Hypertrophic cardiomyopathy with genetic marker (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2013. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2950982017 Hypertrophic cardiomyopathy with genetic marker (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2950983010 Hypertrophic cardiomyopathy with genetic marker en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3623571000052119 hypertrofisk kardiomyopati med genetisk markör sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic cardiomyopathy with genetic marker (disorder) Is a Hypertrophic cardiomyopathy true Inferred relationship Some
Hypertrophic cardiomyopathy with genetic marker (disorder) Associated morphology Hypertrophy true Inferred relationship Some 1
Hypertrophic cardiomyopathy with genetic marker (disorder) Finding site Myocardium structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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