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763070001: Autosomal dominant spastic paraplegia type 42 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3637770011 Autosomal dominant spastic paraplegia type 42 en Synonym Active Entire term case insensitive SNOMED CT core module
3637771010 Autosomal dominant spastic paraplegia type 42 (disorder) en Fully specified name 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 42 Is a Pure hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 42 Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 42 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 42 Finding site Spinal cord structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 42 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 Associated morphology Degenerative abnormality false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 42 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 42 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 42 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 42 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 4
Autosomal dominant spastic paraplegia type 42 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal dominant spastic paraplegia type 42 Interprets Movement observable true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 42 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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