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763374004: Autosomal dominant spastic paraplegia type 12 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3640260011 Autosomal dominant spastic paraplegia type 12 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640261010 Autosomal dominant spastic paraplegia type 12 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404046016 A pure form of hereditary spastic paraplegia characterized by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404047013 A pure form of hereditary spastic paraplegia characterised by a childhood- to adulthood-onset of slowly progressive lower limb spasticity and hyperreflexia of lower extremities, extensor plantar reflexes, distal sensory impairment, variable urinary dysfunction and pes cavus. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant spastic paraplegia type 12 (disorder) Is a Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 12 (disorder) Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 12 (disorder) Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 12 (disorder) Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Associated morphology Degeneration false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Spinal cord structure false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Lower limb structure false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 12 (disorder) Associated morphology Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Lower limb structure false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 12 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 12 (disorder) Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 12 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 12 (disorder) Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) Has interpretation Absent true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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