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732948003: Autosomal dominant spastic paraplegia type 10 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3498419013 Autosomal dominant spastic paraplegia type 10 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3498420019 Autosomal dominant spastic paraplegia type 10 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 10 Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 10 Is a Hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 10 Occurrence Congenital false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 10 Finding site Lower limb structure false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 10 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 10 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 10 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 10 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 10 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 10 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 10 Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 10 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 10 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 10 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 10 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 10 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 10 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 4
Autosomal dominant spastic paraplegia type 10 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal dominant spastic paraplegia type 10 Interprets Movement observable true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 10 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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