FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

763369007: paraplégie spastique autosomique dominante type 37 (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
3640243018 Autosomal dominant spastic paraplegia type 37 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640244012 Autosomal dominant spastic paraplegia type 37 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765961000241111 paraplégie spastique autosomique dominante type 37 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
938641000172117 paraplégie spastique autosomique dominante type 37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
940841000172119 SPG37 - spastic paraplegia type 37 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3640245013 A pure form of hereditary spastic paraplegia with a childhood to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients. 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 37 (disorder) morphologie associée (attribut) Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 37 (disorder) localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) 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

Back to Start