54280009: Kugelberg-Welander disease (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease
• \Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Kugelberg-Welander disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1231316010	Spinal muscular atrophy type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
198509013	Spinal muscular atrophy, type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
198510015	SMA3	en	Synonym	Active	Case sensitive	SNOMED CT core
198511016	SMA type III	en	Synonym	Active	Case sensitive	SNOMED CT core
792493019	Kugelberg-Welander disease (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
90227012	Kugelberg-Welander disease	en	Synonym	Active	Case sensitive	SNOMED CT core
90228019	Familial spinal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
90229010	Juvenile spinal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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