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715491000: Autosomal recessive spastic paraplegia type 11 (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302804012 Autosomal recessive spastic paraplegia type 11 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3302805013 Autosomal recessive spastic paraplegia type 11 en Synonym Active Case insensitive SNOMED CT core
3302806014 Nakamura Osame syndrome en Synonym Active Case sensitive SNOMED CT core
3302807017 Spastic paraplegia, intellectual disability and thin corpus callosum en Synonym Active Case insensitive SNOMED CT core
3302808010 Progressive weakness and spasticity of the lower limbs due to degeneration of corticospinal axons. Autosomal recessive spastic paraplegia type 11 is a form of complicated spastic paraplegia with neurological features such as mental impairment and thin corpus callosum in addition to spasticity. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 11 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 11 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 11 Clinical course Progressive true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 11 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 11 Finding site Structure of right lower limb true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 11 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 11 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 11 Has interpretation Absent true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 11 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 11 Is a Complicated hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Some
Autosomal recessive spastic paraplegia type 11 Finding site Structure of lower limb false Inferred relationship Some
Autosomal recessive spastic paraplegia type 11 Associated morphology Degeneration false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 11 Finding site Spinal cord structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 11 Finding site Cerebellar structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 11 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 11 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 11 Finding site Structure of lower limb false Inferred relationship Some 2

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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