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2816000: Dilated cardiomyopathy due to myotonic dystrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5757011 Dilated cardiomyopathy secondary to myotonic dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
4545813016 Dilated cardiomyopathy due to myotonic dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4545814010 Dilated cardiomyopathy due to myotonic dystrophy 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
Dilated cardiomyopathy due to myotonic dystrophy Is a Dilated cardiomyopathy due to neuromuscular disorder false Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to myotonic dystrophy Finding site Myocardium structure false Inferred relationship Existential restriction modifier 1
Dilated cardiomyopathy due to myotonic dystrophy Associated morphology Dystrophy false Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to myotonic dystrophy Associated morphology Dilatation false Inferred relationship Existential restriction modifier 1
Dilated cardiomyopathy due to myotonic dystrophy Is a Cardiomyopathy in myotonic dystrophy true Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to myotonic dystrophy Associated with Steinert myotonic dystrophy syndrome false Inferred relationship Existential restriction modifier 2
Dilated cardiomyopathy due to myotonic dystrophy Finding site Myocardium structure true Inferred relationship Existential restriction modifier 1
Dilated cardiomyopathy due to myotonic dystrophy Associated morphology Dilatation true Inferred relationship Existential restriction modifier 1
Dilated cardiomyopathy due to myotonic dystrophy Is a Dilated cardiomyopathy due to muscular dystrophy true Inferred relationship Existential restriction modifier
Dilated cardiomyopathy due to myotonic dystrophy Due to Steinert myotonic dystrophy syndrome false Inferred relationship Existential restriction modifier 2
Dilated cardiomyopathy due to myotonic dystrophy Due to Myotonic dystrophy true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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