111499002: Déjérine-Sottas disease (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Peripheral nerve finding\Peripheral nerve disease\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
\General finding of soft tissue\Disorder of soft tissue\Peripheral nerve disease\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\Disorder of nervous system\Neuropathy\Peripheral nerve disease\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Peripheral nerve disease\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the peripheral nervous system\Hereditary peripheral neuropathy\Hereditary motor and sensory neuropathy\Déjérine-Sottas disease
\Disease\Disorder of soft tissue\Peripheral nerve disease\Peripheral demyelinating neuropathy\Hypertrophic interstitial neuropathy\Déjérine-Sottas disease

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

Descriptions:

Id Description Lang Type Status Case? Module

178741012 Déjérine-Sottas disease en Synonym Active Entire term case sensitive SNOMED CT core module

187822012 Hereditary sensory-motor neuropathy, type III en Synonym Active Only initial character case insensitive SNOMED CT core module

187823019 Hereditary hypertrophic neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

187824013 Dejerine-Sottas disease en Synonym Active Entire term case sensitive SNOMED CT core module

187825014 Progressive hypertrophic interstitial neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

199738016 Hereditary motor and sensory neuropathy, type III en Synonym Active Only initial character case insensitive SNOMED CT core module

199739012 HSMN III en Synonym Active Entire term case sensitive SNOMED CT core module

199740014 HMSN III en Synonym Active Entire term case sensitive SNOMED CT core module

632191012 Déjérine-Sottas disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1219654012 Hypertrophic hereditary neuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

1219655013 Hereditary motor and sensory neuropathy type III en Synonym Active Only initial character case insensitive SNOMED CT core module

1219656014 Hypertrophic demyelinative neuropathy of infancy en Synonym Active Entire term case insensitive SNOMED CT core module

4011887018 Charcot-Marie-Tooth disease type 3 en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Déjérine-Sottas disease	Is a	Hereditary motor and sensory neuropathy	false	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Is a	Hypertrophic interstitial neuropathy	true	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier	2
Déjérine-Sottas disease	Finding site	Nerve structure	false	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Associated morphology	Hypertrophy	false	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Is a	Neuropathy	false	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Is a	Hereditary motor and sensory neuropathy	true	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Is a	Neuropathy	false	Inferred relationship	Existential restriction modifier
Déjérine-Sottas disease	Finding site	Neurilemma	false	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Associated morphology	Hypertrophy	false	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Finding site	Neurilemma	false	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Finding site	Peripheral nervous system structure	false	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier	2
Déjérine-Sottas disease	Associated morphology	Remyelination	true	Inferred relationship	Existential restriction modifier	1
Déjérine-Sottas disease	Finding site	Peripheral nerve structure	true	Inferred relationship	Existential restriction modifier	3
Déjérine-Sottas disease	Associated morphology	Segmental demyelination	true	Inferred relationship	Existential restriction modifier	3
Déjérine-Sottas disease	Associated morphology	Hypertrophy	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Roussy-Levy syndrome	Is a	False	Déjérine-Sottas disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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