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193237003: spierziekte met myotonie (aandoening)


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
297624013 Myotonic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
577102013 Myotonic disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
13231000146114 spierziekte met myotonie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
78811000146115 myotone aandoening nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
953361000146113 spierziekte met myotonie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7097901000146118 myotonie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7550261000146118 Dit zijn spierziekten met als kenmerken een te langzame en onvolledige ontspanning van de spieren na samentrekking. nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myotonic disorder Is a Disorder of skeletal muscle true Inferred relationship Some
Myotonic disorder Finding site Skeletal muscle structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital myotonia, autosomal recessive form Is a False Myotonic disorder Inferred relationship Some
Paramyotonia congenita Is a True Myotonic disorder Inferred relationship Some
Congenital myotonia, autosomal dominant form Is a False Myotonic disorder Inferred relationship Some
Steinert myotonic dystrophy syndrome Is a False Myotonic disorder Inferred relationship Some
Infantile myotonia Is a True Myotonic disorder Inferred relationship Some
Other specified myotonic disorder Is a False Myotonic disorder Inferred relationship Some
Myotonic disorder NOS Is a False Myotonic disorder Inferred relationship Some
Congenital myotonic dystrophy Is a False Myotonic disorder Inferred relationship Some
Non dystrophic myotonia (disorder) Is a True Myotonic disorder Inferred relationship Some
Myotonia caused by drug Is a True Myotonic disorder Inferred relationship Some
Potassium aggravated myotonia (disorder) Is a True Myotonic disorder Inferred relationship Some
Rippling muscle disease (disorder) Is a True Myotonic disorder Inferred relationship Some
Proximal myotonic myopathy (disorder) Is a False Myotonic disorder Inferred relationship Some
Myotonia congenita (disorder) Is a True Myotonic disorder Inferred relationship Some
Richieri Costa-da Silva syndrome Is a True Myotonic disorder Inferred relationship Some
Myotonic dystrophy (disorder) Is a True Myotonic disorder Inferred relationship Some
proximale myotone myopathie Is a False Myotonic disorder Inferred relationship Some
Autoimmune rippling muscle disease (disorder) Is a False Myotonic disorder Inferred relationship Some
Hereditary rippling muscle disease (disorder) Is a False Myotonic disorder Inferred relationship Some
congenitale myotonie (aandoening) Is a False Myotonic disorder Inferred relationship Some

Reference Sets

Dutch rare neuromuscular disorders simple reference set (foundation metadata concept)

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