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698292000: Chronic paraplegia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2973815010 Chronic paraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2973818012 Chronic paraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2973815010 Chronic paraplegia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2973815010 Chronic paraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2973818012 Chronic paraplegia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2973818012 Chronic paraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5865181000241117 paraplégie chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5865181000241117 paraplégie chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


98 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic paraplegia (disorder) Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic paraplegia (disorder) Is a Paraplegia true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic paraplegia (disorder) Clinical course Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic paraplegia (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic paraplegia (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Chronic paraplegia (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 5
Chronic paraplegia (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Chronic paraplegia (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Chronic paraplegia (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic paraplegia (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant spastic paraplegia type 8 Is a False Chronic paraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
SPOAN and SPOAN-related disorder Is a False Chronic paraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare complex hereditary spastic paraplegia characterised by neonatal to infantile onset of progressive spasticity in the lower limbs, hyperreflexia, tip-toe walking, pes equinus, and delayed motor developmental milestones. Kyphoscoliosis becomes evident in older patients, and most patients show atrophy of the lateral aspects of the tongue. Additional signs may include intellectual disability, language impairment, and moderate upper limb involvement. Is a False Chronic paraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 76 is a rare, complex hereditary spastic paraplegia characterized by adult onset slowly progressive, mild to moderate lower limb spasticity and hyperreflexia, resulting in gait disturbances, commonly associated with upper limb hyperreflexia and dysarthria. Foot deformities (usually pes cavus) and extensor plantar responses are also frequent. Additional features may include ataxia, lower limb weakness/amyotrophy, abnormal bladder function, distal sensory loss and mild intellectual deterioration. Is a False Chronic paraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spastic paraplegia Is a True Chronic paraplegia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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