FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

230263009: Autosomal dominant spastic paraplegia type 17 (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
345081017 Silver disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4674028016 A complex hereditary spastic paraplegia with characteristics of progressive spastic paraplegia, upper and lower limb muscle atrophy, hyperreflexia, extensor plantar responses, pes cavus and occasionally impaired vibration sense. 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 17 (disorder) Is a Disorder primarily affecting the motor pathways false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Lower limb structure false Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) Associated morphology Degeneration false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) Occurrence Congenital false Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Peripheral nervous system structure true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant distal hereditary motor neuropathy (disorder) true Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Nerve structure true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 17 (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Complicated hereditary spastic paraplegia false Inferred relationship Some
Autosomal dominant spastic paraplegia type 17 (disorder) Interprets Movement true Inferred relationship Some 8
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Structure of right lower limb (body structure) true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 17 (disorder) Finding site Structure of left lower limb (body structure) true Inferred relationship Some 7
Autosomal dominant spastic paraplegia type 17 (disorder) Interprets Movement observable true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 17 (disorder) Has interpretation Absent true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 17 (disorder) Is a Autosomal dominant complex hereditary spastic paraplegia (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start