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1172631001: Autosomal recessive spastic paraplegia type 76 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4634876010 Autosomal recessive spastic paraplegia type 76 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4634878011 Autosomal recessive spastic paraplegia type 76 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 76 Is a Complicated hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 76 Is a Chronic paraplegia false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 76 Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 76 Clinical course Progressive true Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 76 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 76 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 76 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 76 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 76 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 76 Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Autosomal recessive spastic paraplegia type 76 Interprets Movement true Inferred relationship Existential restriction modifier 6
Autosomal recessive spastic paraplegia type 76 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 76 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 5
Autosomal recessive spastic paraplegia type 76 Interprets Movement observable true Inferred relationship Existential restriction modifier 4
Autosomal recessive spastic paraplegia type 76 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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