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195031006: Cardiomyopathy in myotonic dystrophy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
300054017 Cardiomyopathy in myotonic dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
579080012 Cardiomyopathy in myotonic dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4853781000241115 cardiomyopathie dans la dystrophie myotonique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cardiomyopathy in myotonic dystrophy Is a affection spécifique du muscle cardiaque false Inferred relationship Some
Cardiomyopathy in myotonic dystrophy Finding site Myocardium structure true Inferred relationship Some 2
Cardiomyopathy in myotonic dystrophy Is a Cardiomyopathy false Inferred relationship Some
Cardiomyopathy in myotonic dystrophy 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 1
Cardiomyopathy in myotonic dystrophy Is a Cardiomyopathy associated with another disorder (disorder) true Inferred relationship Some
Cardiomyopathy in myotonic dystrophy Associated with Myotonic dystrophy (disorder) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Dilated cardiomyopathy due to myotonic dystrophy (disorder) Is a True Cardiomyopathy in myotonic dystrophy Inferred relationship Some

This concept is not in any reference sets

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