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763069002: paraplégie spastique autosomique dominante type 41 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1001251000172113 SPG41 - spastic paraplegia type 41 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3637767012 Autosomal dominant spastic paraplegia type 41 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3637768019 Autosomal dominant spastic paraplegia type 41 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765511000241116 paraplégie spastique autosomique dominante type 41 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
977961000172113 paraplégie spastique autosomique dominante type 41 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3637769010 A pure form of hereditary spastic paraplegia with onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise. 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 41 (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 41 (disorder) est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 41 (disorder) est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 41 (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 (disorder) localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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