111499002: Déjérine-Sottas disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Peripheral nerve finding\Peripheral neuropathy\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
• \General finding of soft tissue\Disorder of soft tissue\Peripheral neuropathy\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
• \Disease\Degenerative disorder\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of body system\Neurological disorder\Neuropathy\Peripheral neuropathy\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Peripheral neuropathy\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
• \Disease\Disorder of soft tissue\Peripheral neuropathy\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1219654012	Hypertrophic hereditary neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
1219655013	Hereditary motor and sensory neuropathy type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
1219656014	Hypertrophic demyelinative neuropathy of infancy	en	Synonym	Active	Case insensitive	SNOMED CT core
178741012	Déjérine-Sottas disease	en	Synonym	Active	Case sensitive	SNOMED CT core
187822012	Hereditary sensory-motor neuropathy, type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
187823019	Hereditary hypertrophic neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
187824013	Dejerine-Sottas disease	en	Synonym	Active	Case sensitive	SNOMED CT core
187825014	Progressive hypertrophic interstitial neuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
199738016	Hereditary motor and sensory neuropathy, type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
199739012	HSMN III	en	Synonym	Active	Case sensitive	SNOMED CT core
199740014	HMSN III	en	Synonym	Active	Case sensitive	SNOMED CT core
4011887018	Charcot-Marie-Tooth disease type 3	en	Synonym	Active	Case sensitive	SNOMED CT core
632191012	Déjérine-Sottas disease (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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