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230263009: paraplégie spastique autosomique dominante type 17 (trouble)


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
345081017 Silver disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
546491000241111 paraplégie spastique autosomique dominante type 17 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
950031000172116 SPG17 - spastic paraplegia type 17 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
991741000172112 paraplégie spastique autosomique dominante type 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
4674028016 A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. en Definition 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
Autosomal dominant spastic paraplegia type 17 (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) localisation d'une constatation (attribut) structure du système nerveux périphérique true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 17 (disorder) est un(e) (attribut) Autosomal dominant distal hereditary motor neuropathy (disorder) true Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) localisation d'une constatation (attribut) structure d'un nerf true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 17 (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 17 (disorder) est un(e) (attribut) Complicated hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) est un(e) (attribut) Disorder primarily affecting the motor pathways (disorder) false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) localisation d'une constatation (attribut) système nerveux false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 17 (disorder) est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) survenue (attribut) congénital false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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