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719103009: Autosomal recessive spastic paraplegia type 39 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3314993016 Autosomal recessive spastic paraplegia type 39 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3314994010 Autosomal recessive spastic paraplegia type 39 en Synonym Active Case insensitive SNOMED CT core
3314995011 Spastic paraplegia due to neuropathy target esterase mutation en Synonym Active Case insensitive SNOMED CT core
3314997015 Spastic paraplegia due to NTE (neuropathy target esterase) mutation en Synonym Active Initial character case insensitive SNOMED CT core
3314996012 This syndrome has characteristics of progressive spastic paraplegia and distal muscle wasting. So far, it has been described in two families. All affected individuals carried mutations in the neuropathy target esterase (NTE) gene, encoding a neural membrane protein. 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 39 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 39 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 39 Clinical course Progressive true Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 39 Interprets Movement true Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 39 Finding site Structure of right lower limb true Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 39 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 39 Interprets Movement observable true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 39 Has interpretation Absent true Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 39 Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Autosomal recessive spastic paraplegia type 39 Is a Complicated hereditary spastic paraplegia true Inferred relationship Some
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Some
Autosomal recessive spastic paraplegia type 39 Finding site Structure of lower limb false Inferred relationship Some
Autosomal recessive spastic paraplegia type 39 Associated morphology Degeneration false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 39 Finding site Spinal cord structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 39 Finding site Cerebellar structure false Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 39 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 39 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 39 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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