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763070001: paraplégie spastique autosomique dominante type 42 (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
3637770011 Autosomal dominant spastic paraplegia type 42 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3637771010 Autosomal dominant spastic paraplegia type 42 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
765521000241111 paraplégie spastique autosomique dominante type 42 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
880181000172115 paraplégie spastique autosomique dominante type 42 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
972431000172114 SPG42 - spastic paraplegia type 42 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3637772015 A pure form of hereditary spastic paraplegia with characteristics of slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging. 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 42 morphologie associée (attribut) Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 42 évolution clinique (attribut) progressif true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 42 localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 42 localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 42 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 42 est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 42 est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 42 survenue (attribut) congénital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 42 survenue (attribut) congénital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 42 localisation d'une constatation (attribut) moelle spinale (structure corporelle) false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 42 localisation d'une constatation (attribut) membre inférieur false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 42 morphologie associée (attribut) dégénérescence 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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