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230263009: Autosomal dominant spastic paraplegia type 17 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345081017 Silver disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674028016 A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
345081017 Silver disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345081017 Silver disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
345081017 Silver disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
618047012 Silver disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618047012 Silver disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674028016 A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3384961001000114 Spastische Paraplegie, autosomal-dominante, Typ 17 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950031000172116 SPG17 - spastic paraplegia type 17 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
991741000172112 paraplégie spastique autosomique dominante type 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
950031000172116 SPG17 - spastic paraplegia type 17 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
991741000172112 paraplégie spastique autosomique dominante type 17 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3384961001000114 Spastische Paraplegie, autosomal-dominante, Typ 17 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Disorders primarily affecting the motor pathways false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant spastic paraplegia type 17 (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant spastic paraplegia type 17 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant spastic paraplegia type 17 (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant distal hereditary motor neuropathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Autosomal dominant spastic paraplegia type 17 (disorder) Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 5
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Complicated hereditary spastic paraplegia (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 17 (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 8
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 7
Autosomal dominant spastic paraplegia type 17 (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 17 (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant complex hereditary spastic paraplegia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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