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111499002: Déjérine-Sottas disease (disorder)


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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Déjérine-Sottas disease localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 1
Déjérine-Sottas disease localisation d'une constatation (attribut) nerf périphérique (structure corporelle) true Inferred relationship Some 1
Déjérine-Sottas disease localisation d'une constatation (attribut) nerf périphérique (structure corporelle) true Inferred relationship Some 2
Déjérine-Sottas disease morphologie associée (attribut) Remyelination true Inferred relationship Some 1
Déjérine-Sottas disease localisation d'une constatation (attribut) nerf périphérique (structure corporelle) true Inferred relationship Some 3
Déjérine-Sottas disease morphologie associée (attribut) Segmental demyelination true Inferred relationship Some 3
Déjérine-Sottas disease morphologie associée (attribut) hypertrophie true Inferred relationship Some 2
Déjérine-Sottas disease est un(e) (attribut) Neuropathy false Inferred relationship Some
Déjérine-Sottas disease est un(e) (attribut) Hereditary motor and sensory neuropathy (disorder) true Inferred relationship Some
Déjérine-Sottas disease est un(e) (attribut) Neuropathy (disorder) false Inferred relationship Some
Déjérine-Sottas disease localisation d'une constatation (attribut) Neurilemma false Inferred relationship Some 1
Déjérine-Sottas disease morphologie associée (attribut) hypertrophie false Inferred relationship Some 1
Déjérine-Sottas disease localisation d'une constatation (attribut) Neurilemma false Inferred relationship Some 1
Déjérine-Sottas disease localisation d'une constatation (attribut) structure du système nerveux périphérique false Inferred relationship Some 2
Déjérine-Sottas disease localisation d'une constatation (attribut) structure d'un nerf false Inferred relationship Some
Déjérine-Sottas disease morphologie associée (attribut) hypertrophie false Inferred relationship Some 1
Déjérine-Sottas disease est un(e) (attribut) Hereditary motor and sensory neuropathy false Inferred relationship Some
Déjérine-Sottas disease est un(e) (attribut) neuropathie interstitielle hypertrophique true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Roussy-Levy syndrome est un(e) (attribut) False Déjérine-Sottas disease Inferred relationship Some

This concept is not in any reference sets

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