230556005: X-linked recessive sensory neuropathy (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 sensory neuropathy\X-linked recessive sensory neuropathy
• \Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\X-linked recessive sensory neuropathy
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary sensory neuropathy\X-linked recessive sensory neuropathy
• \Disorder of body system\Neurological disorder\Neuropathy\Sensory neuropathy\Hereditary sensory neuropathy\X-linked recessive sensory neuropathy
• \Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary sensory neuropathy\X-linked recessive sensory neuropathy
• \Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Hereditary sensory neuropathy\X-linked recessive sensory neuropathy

Status: current, Defined. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345466015	X-linked recessive sensory neuropathy	en	Synonym	Active	Case sensitive	SNOMED CT core
618382019	X-linked recessive sensory neuropathy (disorder)	en	Fully specified name	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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