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2816000: Dilated cardiomyopathy due to myotonic dystrophy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
5757011 Dilated cardiomyopathy secondary to myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4545813016 Dilated cardiomyopathy due to myotonic dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4545814010 Dilated cardiomyopathy due to myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4397811000241117 cardiomyopathie dilatée secondaire à une dystrophie myotonique fr Synonym (core metadata concept) Active Entire term 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
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Is a Dilated cardiomyopathy due to neuromuscular disorder (disorder) false Inferred relationship Some
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Finding site Myocardium structure false Inferred relationship Some 1
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Associated morphology Dystrophy false Inferred relationship Some
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Associated morphology Dilatation false Inferred relationship Some 1
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Is a Cardiomyopathy in myotonic dystrophy true Inferred relationship Some
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Associated with A rare genetic multi-system disorder characterised by a wide range of muscle-related manifestations (muscle weakness, myotonia, early onset cataracts before age 50) and systemic manifestations (cerebral, endocrine, cardiac, gastrointestinal tract, uterus, skin and immunologic involvement) that vary depending on the age of onset. The very wide clinical spectrum ranges from lethal presentations in infancy to mild, late-onset disease. false Inferred relationship Some 2
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Finding site Myocardium structure true Inferred relationship Some 1
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Associated morphology Dilatation true Inferred relationship Some 1
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Is a Dilated cardiomyopathy due to muscular dystrophy (disorder) true Inferred relationship Some
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Due to A rare genetic multi-system disorder characterised by a wide range of muscle-related manifestations (muscle weakness, myotonia, early onset cataracts before age 50) and systemic manifestations (cerebral, endocrine, cardiac, gastrointestinal tract, uterus, skin and immunologic involvement) that vary depending on the age of onset. The very wide clinical spectrum ranges from lethal presentations in infancy to mild, late-onset disease. false Inferred relationship Some 2
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Due to Myotonic dystrophy (disorder) true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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