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763376002: paraplégie spastique autosomique récessive type 28 (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
3640266017 Autosomal recessive spastic paraplegia type 28 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640267014 Autosomal recessive spastic paraplegia type 28 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
766011000241115 paraplégie spastique autosomique récessive type 28 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
946311000172113 SPG28 - spastic paraplegia type 28 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
969391000172115 paraplégie spastique autosomique récessive type 28 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3640268016 A pure form of hereditary spastic paraplegia with a childhood or adolescent onset of slowly progressive, pure crural muscle spastic paraparesis which manifests with mild lower limb weakness, gait difficulties, extensor plantar responses, and hyperreflexia of lower extremities. Less common manifestations reported include cerebellar oculomotor disturbance with saccadic eye pursuit, pes cavus and scoliosis. Some patients also present pin and vibration sensory loss in distal legs. The disease is caused by homozygous or compound heterozygous mutation in the DDHD1 gene on chromosome 14q22. 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 28 morphologie associée (attribut) Degenerative abnormality false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 est un(e) (attribut) Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 28 évolution clinique (attribut) progressif true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 28 localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 28 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 28 est un(e) (attribut) Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 28 est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 28 survenue (attribut) congénital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 28 survenue (attribut) congénital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 localisation d'une constatation (attribut) moelle spinale (structure corporelle) false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 morphologie associée (attribut) dégénérescence false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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