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763375003: Autosomal dominant spastic paraplegia type 19 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3640263013 Autosomal dominant spastic paraplegia type 19 en Synonym Active Case insensitive SNOMED CT core
3640264019 Autosomal dominant spastic paraplegia type 19 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3640265018 A pure form of hereditary spastic paraplegia with characteristics of a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy. 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 19 Associated morphology Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Clinical course Progressive true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 19 Finding site Structure of lower limb false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 19 Finding site Structure of right lower limb true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 19 Finding site Structure of left lower limb true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 19 Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Has interpretation Absent true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Is a Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 19 Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 19 Finding site Structure of lower limb false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 Associated morphology Degeneration false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 19 Finding site Spinal cord structure false Inferred relationship Some 2

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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