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230263009: Autosomal dominant spastic paraplegia type 17 (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345081017 Silver disease en Synonym Active Case sensitive SNOMED CT core
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Silver disease Associated morphology Degenerative abnormality true Inferred relationship Some 1
Silver disease Finding site Peripheral nervous system structure true Inferred relationship Some 3
Silver disease Is a Autosomal dominant distal hereditary motor neuropathy true Inferred relationship Some
Silver disease Finding site Nerve structure true Inferred relationship Some 4
Silver disease Clinical course Progressive true Inferred relationship Some 5
Silver disease Is a Complicated hereditary spastic paraplegia false Inferred relationship Some
Silver disease Interprets Movement true Inferred relationship Some 8
Silver disease Finding site Structure of right lower limb true Inferred relationship Some 6
Silver disease Finding site Structure of left lower limb true Inferred relationship Some 7
Silver disease Interprets Movement observable true Inferred relationship Some 2
Silver disease Has interpretation Absent true Inferred relationship Some 2
Silver disease Is a Autosomal dominant complex hereditary spastic paraplegia true Inferred relationship Some
Silver disease Is a Disorder primarily affecting the motor pathways false Inferred relationship Some
Silver disease Finding site Structure of nervous system false Inferred relationship Some
Silver disease Finding site Structure of lower limb false Inferred relationship Some 2
Silver disease Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Some
Silver disease Finding site Spinal cord structure true Inferred relationship Some 1
Silver disease Associated morphology Degeneration false Inferred relationship Some 1
Silver disease Occurrence Congenital false Inferred relationship Some 1

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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