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715776003: Spastic paraplegia type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303678016 Spastic paraplegia type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303679012 Spastic paraplegia type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303680010 A form of hereditary spastic paraplegia with onset usually in adulthood of progressive bilateral lower limb weakness and spasticity, sphincter dysfunction, decreased vibratory sense at the ankles and with additional manifestations including optical neuropathy, nystagmus, strabismus, decreased hearing, scoliosis, pes cavus, motor and sensory neuropathy, amyotrophy, blepharoptosis and ophthalmoplegia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
872371000172110 paraplégie spastique type 7 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
910251000172111 SPG7 - spastic paraplegia type 7 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
884591000172117 autosomaal recessieve spastische paraplegie type 7 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
918471000172119 SPG7 - spastische paraplegie type 7 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spastic paraplegia type 7 (disorder) Is a Hereditary spastic paraplegia false Inferred relationship Some
Spastic paraplegia type 7 (disorder) Occurrence Congenital false Inferred relationship Some
Spastic paraplegia type 7 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Some 2
Spastic paraplegia type 7 (disorder) Associated morphology Degeneration false Inferred relationship Some 3
Spastic paraplegia type 7 (disorder) Finding site Spinal cord structure false Inferred relationship Some 3
Spastic paraplegia type 7 (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Spastic paraplegia type 7 (disorder) Associated morphology Degeneration false Inferred relationship Some 1
Spastic paraplegia type 7 (disorder) Occurrence Congenital false Inferred relationship Some 1
Spastic paraplegia type 7 (disorder) Finding site Spinal cord structure true Inferred relationship Some 1
Spastic paraplegia type 7 (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Some
Spastic paraplegia type 7 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Spastic paraplegia type 7 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Spastic paraplegia type 7 (disorder) Is a Autosomal recessive hereditary spastic paraplegia true Inferred relationship Some
Spastic paraplegia type 7 (disorder) Is a Ataxia of bilateral lower limbs (finding) true Inferred relationship Some
Spastic paraplegia type 7 (disorder) Interprets Movement true Inferred relationship Some 6
Spastic paraplegia type 7 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Some 2
Spastic paraplegia type 7 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Some 4
Spastic paraplegia type 7 (disorder) Interprets Movement observable true Inferred relationship Some 5
Spastic paraplegia type 7 (disorder) Has interpretation Absent true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Belgian subset for medical problems in patient health records

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