267607008: Familial periodic paralysis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis
• \Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis
• \Disease\Myopathy\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Metabolic myopathy\Familial periodic paralysis

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
399422014	Familial periodic paralysis	en	Synonym	Active	Case insensitive	SNOMED CT core
399423016	Myoplegic dystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
399424010	Familial recurrent paralysis	en	Synonym	Active	Case insensitive	SNOMED CT core
399425011	Familial myoplegia	en	Synonym	Active	Case insensitive	SNOMED CT core
399427015	Cavarre disease	en	Synonym	Active	Case sensitive	SNOMED CT core
399428013	Periodic myotonia	en	Synonym	Active	Case insensitive	SNOMED CT core
660244012	Familial periodic paralysis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Emergency department reference set

Australian emergency department reference set

NSW Emergency Department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Emergency department diagnosis reference set

Problem/Diagnosis reference set

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