128212001: Spinal muscular atrophy, type II (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\Spinal muscular atrophy, type II
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal muscular atrophy, type II
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal muscular atrophy, type II
• \Disorder of body system\Neurological disorder\Motor neurone disease\Lower motor neuron disease\Spinal muscular atrophy\Spinal muscular atrophy, type II
• \Disorder of body system\Neurological disorder\Motor neurone disease\Hereditary motor neuron disease\Spinal muscular atrophy\Spinal muscular atrophy, type II

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
206455015	SMA2	en	Synonym	Active	Case sensitive	SNOMED CT core
206456019	Late infantile spinal muscular atrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
206457011	Spinal muscular atrophy, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474347015	Spinal muscular atrophy type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
732178012	Spinal muscular atrophy, type II (disorder)	en	Fully specified name	Active	Initial character 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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