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763375003: paraplégie spastique autosomique dominante type 19 (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
3640263013 Autosomal dominant spastic paraplegia type 19 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640264019 Autosomal dominant spastic paraplegia type 19 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
766001000241117 paraplégie spastique autosomique dominante type 19 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
938541000172118 SPG19 - spastic paraplegia type 19 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
953171000172110 paraplégie spastique autosomique dominante type 19 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3640265018 A pure form of hereditary spastic paraplegia with characteristics of a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy. 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 19 morphologie associée (attribut) Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 évolution clinique (attribut) progressif true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 19 localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 19 est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 19 localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 morphologie associée (attribut) dégénérescence false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 survenue (attribut) congénital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 survenue (attribut) congénital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 localisation d'une constatation (attribut) moelle spinale (structure corporelle) false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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