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471885006: Hypertrophic cardiomyopathy with genetic marker (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2950982017 Hypertrophic cardiomyopathy with genetic marker (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2950983010 Hypertrophic cardiomyopathy with genetic marker en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic cardiomyopathy with genetic marker Is a Hypertrophic cardiomyopathy true Inferred relationship Existential restriction modifier
Hypertrophic cardiomyopathy with genetic marker Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 1
Hypertrophic cardiomyopathy with genetic marker Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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