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763369007: Autosomal dominant spastic paraplegia type 37 (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
3640243018 Autosomal dominant spastic paraplegia type 37 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640244012 Autosomal dominant spastic paraplegia type 37 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3640245013 A pure form of hereditary spastic paraplegia with 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
938641000172117 paraplégie spastique autosomique dominante type 37 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
940841000172119 SPG37 - spastic paraplegia type 37 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
907961000172117 autosomaal dominante spastische paraplegie type 37 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
944411000172112 SPG37 - spastische paraplegie type 37 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
Autosomal dominant spastic paraplegia type 37 (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) Is a Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) Associated morphology Degeneration false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Spinal cord structure false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Associated morphology Degenerative abnormality false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 37 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Lower limb structure (body structure) false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 37 (disorder) Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 37 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 37 (disorder) Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) Has interpretation Absent true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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