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719103009: Autosomal recessive spastic paraplegia type 39 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3314993016 Autosomal recessive spastic paraplegia type 39 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3314994010 Autosomal recessive spastic paraplegia type 39 en Synonym Active Entire term case insensitive SNOMED CT core module
3314995011 Spastic paraplegia due to neuropathy target esterase mutation en Synonym Active Entire term case insensitive SNOMED CT core module
3314997015 Spastic paraplegia due to NTE (neuropathy target esterase) mutation en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spastic paraplegia type 39 Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 39 Is a Complicated hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 39 Finding site Lower limb structure false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 39 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 39 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 39 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 39 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 39 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 39 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 39 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 39 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 39 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 39 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 39 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal recessive spastic paraplegia type 39 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 39 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal recessive spastic paraplegia type 39 Interprets Movement observable true Inferred relationship Existential restriction modifier 4
Autosomal recessive spastic paraplegia type 39 Has interpretation Absent true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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