1230343006: Distal hereditary motor neuropathy type 2 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Disorder of body system\Neurological disorder\Neuropathy\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Disorder of body system\Neurological disorder\Chronic nervous system disorder\Distal hereditary motor neuropathy type 2
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy\Distal hereditary motor neuropathy type 2
• \Chronic disease\Chronic nervous system disorder\Distal hereditary motor neuropathy type 2

Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5069342019	Distal hereditary motor neuropathy type 2 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5069343012	Autosomal dominant distal spinal muscular atrophy type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
5069344018	Distal hereditary motor neuropathy type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
5069345017	A rare autosomal dominant distal hereditary motor neuropathy with characteristics of onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. Sensory involvement is typically less pronounced or absent. The severity of the condition is variable and both lower and upper extremities may be involved.	en	Definition	Active	Case sensitive	SNOMED CT core

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