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783622001: Autosomal dominant spastic paraplegia type 38 (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759543016 Autosomal dominant spastic paraplegia type 38 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3759544010 Autosomal dominant spastic paraplegia type 38 en Synonym Active Case insensitive SNOMED CT core
3759545011 A complex hereditary spastic paraplegia with characteristics of mild to severe lower limbs spasticity, hyperreflexia, extensor plantar responses, pes cavus and significant wasting and weakness of the small hand muscles. Impaired vibration sensation, temporal lobe epilepsy and cognitive dysfunction were also reported. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant spastic paraplegia type 38 Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 38 Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 38 Is a Complicated hereditary spastic paraplegia false Inferred relationship Some
Autosomal dominant spastic paraplegia type 38 Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Some
Autosomal dominant spastic paraplegia type 38 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 38 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 38 Finding site Structure of lower limb false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 38 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 38 Clinical course Progressive true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 38 Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 38 Finding site Structure of right lower limb true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 38 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 38 Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 38 Has interpretation Absent true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 38 Is a Autosomal dominant complex hereditary spastic paraplegia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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