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230260007: Pure hereditary spastic paraplegia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345078010 Pure hereditary spastic paraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618044017 Pure hereditary spastic paraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
345078010 Pure hereditary spastic paraplegia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
345078010 Pure hereditary spastic paraplegia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
618044017 Pure hereditary spastic paraplegia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
618044017 Pure hereditary spastic paraplegia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3425891001000112 Hereditäre spastische Paraplegie, reine Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
946961000172110 HSP pure - pure hereditary spastic paraplegia fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981551000172119 paraplégie spastique héréditaire pure fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
946961000172110 HSP pure - pure hereditary spastic paraplegia fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981551000172119 paraplégie spastique héréditaire pure fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3425891001000112 Hereditäre spastische Paraplegie, reine Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pure hereditary spastic paraplegia Is a Hereditary spastic paraplegia true Inferred relationship Existential restriction modifier (core metadata concept)
Pure hereditary spastic paraplegia Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Finding site Spinal cord structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Finding site Lower limb structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Finding site Spinal cord structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Pure hereditary spastic paraplegia Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pure hereditary spastic paraplegia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pure hereditary spastic paraplegia Finding site Spinal cord structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pure hereditary spastic paraplegia Associated morphology Degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pure hereditary spastic paraplegia Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pure hereditary spastic paraplegia Finding site Spinal cord structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pure hereditary spastic paraplegia Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pure hereditary spastic paraplegia Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Pure hereditary spastic paraplegia Finding site Structure of right lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Pure hereditary spastic paraplegia Finding site Structure of left lower limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Pure hereditary spastic paraplegia Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pure hereditary spastic paraplegia Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A pure form of hereditary spastic paraplegia characterized by 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. Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 42 (disorder) Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
A pure form of hereditary spastic paraplegia characterised by a childhood- to adulthood-onset of slowly progressive spastic gait, extensor plantar responses, brisk tendon reflexes in arms and legs, decreased vibration sense at ankles and urinary dysfunction. Ankle clonus is also reported in some patients. Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
X-linked spastic paraplegia type 34 Is a False Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 12 (disorder) Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 19 (disorder) Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 28 Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 71 Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal spastic paraplegia type 72 Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive spastic paraplegia type 24 Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
X-linked pure hereditary spastic paraplegia Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant spastic paraplegia type 73 Is a True Pure hereditary spastic paraplegia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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