764854006: Autosomal dominant slowed nerve conduction velocity (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\Autosomal dominant slowed nerve conduction velocity
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant slowed nerve conduction velocity
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal dominant slowed nerve conduction velocity
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal dominant slowed nerve conduction velocity
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Autosomal dominant slowed nerve conduction velocity
• \Congenital disease\Autosomal dominant slowed nerve conduction velocity

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3655310011	Autosomal dominant slowed nerve conduction velocity	en	Synonym	Active	Case insensitive	SNOMED CT core
3655311010	Autosomal dominant slowed nerve conduction velocity (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3655154010	A hereditary demyelinating motor and sensory neuropathy with characteristics of slowed nerve conduction velocities in the absence of clinically apparent neurological deficits, gait abnormalities or muscular atrophy, associated with a germline mutation in the ARGHEF10 gene.	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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