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782670003: Autosomal dominant spastic paraplegia type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3755087011 Autosomal dominant spastic paraplegia type 3 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3755088018 Autosomal dominant spastic paraplegia type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3755089014 Strumpell disease en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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