64383006: Werdnig-Hoffmann 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\Werdnig-Hoffmann disease
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Werdnig-Hoffmann disease
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Werdnig-Hoffmann disease
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Werdnig-Hoffmann disease
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Anterior horn cell disease\Werdnig-Hoffmann disease
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Werdnig-Hoffmann disease
• \Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Werdnig-Hoffmann disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
107017013	Werdnig-Hoffmann disease	en	Synonym	Active	Case sensitive	SNOMED CT core
107018015	Infantile spinal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
107019011	Progressive muscular atrophy of infancy	en	Synonym	Active	Case insensitive	SNOMED CT core
1232557016	Spinal muscular atrophy type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1232558014	WHD - Werdnig-Hoffmann disease	en	Synonym	Active	Case sensitive	SNOMED CT core
199235017	Spinal muscular atrophy, type I	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
803770017	Werdnig-Hoffmann disease (disorder)	en	Fully specified name	Active	Case sensitive	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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