128207002: Giant axonal neuropathy (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du système nerveux central\Disorder of the central nervous system (disorder)\Axonal neuropathy\Giant axonal neuropathy
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Giant axonal neuropathy
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Neuropathy (disorder)\Axonal neuropathy\Giant axonal neuropathy
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Giant axonal neuropathy
• \Disease\affection d'un système corporel\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Axonal neuropathy\Giant axonal neuropathy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
206449013	Giant axonal neuropathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
518091000241114	neuropathie à axones géants (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
732172013	Giant axonal neuropathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
893851000172112	neuropathie à axones géants	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3777464012	An autosomal recessive condition characterised by progressive degeneration of the central and peripheral nervous system with enlargement of axons.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3777465013	An autosomal recessive condition characterized by progressive degeneration of the central and peripheral nervous system with enlargement of axons.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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