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715491000: Autosomal recessive spastic paraplegia type 11 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302804012 Autosomal recessive spastic paraplegia type 11 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302805013 Autosomal recessive spastic paraplegia type 11 en Synonym Active Entire term case insensitive SNOMED CT core module
3302806014 Nakamura Osame syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3302807017 Spastic paraplegia, intellectual disability and thin corpus callosum en Synonym Active Entire term 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 11 Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 11 Is a Complicated hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 11 Finding site Lower limb structure false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 11 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 11 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 11 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 11 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 11 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 11 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 11 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 11 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 11 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 11 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 11 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal recessive spastic paraplegia type 11 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 11 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal recessive spastic paraplegia type 11 Interprets Movement observable true Inferred relationship Existential restriction modifier 4
Autosomal recessive spastic paraplegia type 11 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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