771143004: Hereditary motor and sensory neuropathy type 5 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy type 5
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary motor and sensory neuropathy type 5
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy type 5
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy type 5
• \Disorder of body system\Neurological disorder\Chronic nervous system disorder\Hereditary motor and sensory neuropathy type 5
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary motor and sensory neuropathy type 5
• \Chronic disease\Chronic nervous system disorder\Hereditary motor and sensory neuropathy type 5

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3704558019	Charcot-Marie-Tooth disease, pyramidal features syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3704559010	Hereditary motor and sensory neuropathy type 5 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3704560017	Hereditary motor and sensory neuropathy type 5	en	Synonym	Active	Case insensitive	SNOMED CT core
3873462011	Hereditary sensory-motor neuropathy type V	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3703840012	A rare axonal hereditary motor and sensory neuropathy with characteristics of slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity.	en	Definition	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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