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783622001: Autosomal dominant spastic paraplegia type 38 (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
3759543016 Autosomal dominant spastic paraplegia type 38 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3759544010 Autosomal dominant spastic paraplegia type 38 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 dominant spastic paraplegia type 38 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 38 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 38 Is a Complicated hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 38 Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 38 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 38 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 38 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 38 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 38 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 38 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 38 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 4
Autosomal dominant spastic paraplegia type 38 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal dominant spastic paraplegia type 38 Interprets Movement observable true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 38 Has interpretation Absent true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 38 Is a Autosomal dominant complex hereditary spastic paraplegia true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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