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763069002: Autosomal dominant spastic paraplegia type 41 (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3637767012 Autosomal dominant spastic paraplegia type 41 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3637768019 Autosomal dominant spastic paraplegia type 41 en Synonym Active Case insensitive SNOMED CT core
3637769010 A pure form of hereditary spastic paraplegia with onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia, spastic gait and mild urinary compromise. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant spastic paraplegia type 41 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 Clinical course Progressive true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 41 Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 41 Finding site Structure of right lower limb true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 41 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 41 Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 Has interpretation Absent true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 Is a Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 41 Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 41 Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 Finding site Structure of lower limb false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 Associated morphology Degeneration false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 41 Finding site Spinal cord structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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