41574007: Paramyotonia congenita (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita
• \Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita
• \Disease\Myopathy\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myotonic disorder\Paramyotonia congenita

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1229775013	Eulenburg's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
1229776014	Eulenburg disease	en	Synonym	Active	Case sensitive	SNOMED CT core
69350017	Paramyotonia congenita	en	Synonym	Active	Case insensitive	SNOMED CT core
69351018	Eulenburg syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
778377012	Paramyotonia congenita (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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