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765753004: paraplégie spastique autosomique récessive type 45 (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
3659583013 Autosomal recessive spastic paraplegia type 45 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3659584019 Autosomal recessive spastic paraplegia type 45 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
767971000241112 paraplégie spastique autosomique récessive type 45 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
932091000172119 paraplégie spastique autosomique récessive type 65 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
958651000172119 paraplégie spastique autosomique récessive type 45 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3658904016 A rare pure or complex form of hereditary spastic paraplegia with characteristics of onset in infancy of progressive lower limb spasticity, abnormal gait, increased deep tendon reflexes and extensor plantar responses that may be associated with intellectual disability. Additional signs such as contractures in the lower limbs, amyotrophy, clubfoot and optic atrophy, have also been reported. Caused by homozygous mutation in the NT5C2 gene on chromosome 10q24. 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 45 (disorder) morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 45 (disorder) est un(e) (attribut) Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 45 (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 45 (disorder) localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 45 (disorder) survenue (attribut) congénital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 45 (disorder) est un(e) (attribut) paraplégie spastique héréditaire (trouble) false Inferred relationship Some
Autosomal recessive spastic paraplegia type 45 (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 45 (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 45 (disorder) localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 45 (disorder) morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 45 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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