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763367009: paraplégie spastique autosomique récessive type 48 (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
3640234010 Autosomal recessive spastic paraplegia type 48 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640235011 Autosomal recessive spastic paraplegia type 48 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765951000241113 paraplégie spastique autosomique récessive type 48 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
922771000172116 SPG48 - spastic paraplegia type 48 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
977291000172112 paraplégie spastique autosomique récessive type 48 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3640236012 A form of hereditary spastic paraplegia with usual characteristics of a pure phenotype of a slowly progressive spastic paraplegia associated with urinary incontinence with an onset in mid to late-adulthood. A complex phenotype, with the additional findings of cognitive impairment, sensorimotor polyneuropathy, ataxia and Parkinsonism as well as thin corpus callosum and white matter lesions (seen on magnetic resonance imaging) has also been reported. 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 recessive spastic paraplegia type 48 (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) est un(e) (attribut) Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 48 (disorder) est un(e) (attribut) paraplégie spastique héréditaire (trouble) false Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 48 (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 48 (disorder) morphologie associée (attribut) dégénérescence 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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