1156837002: Autosomal dominant distal hereditary motor neuropathy (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
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant distal hereditary motor neuropathy
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy
• \Disorder of body system\Neurological disorder\Neuropathy\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Autosomal dominant distal hereditary motor neuropathy
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Peripheral motor neuropathy\Autosomal dominant distal hereditary motor neuropathy

Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4576298019	Autosomal dominant distal hereditary motor neuropathy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4576299010	Autosomal dominant distal hereditary motor neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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