FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
345081017 Silver disease en Synonym Active Entire term case sensitive SNOMED CT core module
618047012 Silver disease (disorder) en Fully specified name Inactive Entire term case insensitive SNOMED CT core module
3701800010 Autosomal dominant spastic paraplegia type 17 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3701801014 Autosomal dominant spastic paraplegia type 17 en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant spastic paraplegia type 17 Is a Disorder primarily affecting the motor pathways false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 17 Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 17 Finding site Lower limb structure false Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 17 Is a Autosomal dominant hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 17 Finding site Spinal cord structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 17 Associated morphology Degeneration false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 17 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 17 Associated morphology Degenerative abnormality true Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 17 Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 17 Is a Autosomal dominant distal hereditary motor neuropathy true Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 17 Finding site Nerve structure true Inferred relationship Existential restriction modifier 4
Autosomal dominant spastic paraplegia type 17 Clinical course Progressive true Inferred relationship Existential restriction modifier 5
Autosomal dominant spastic paraplegia type 17 Is a Complicated hereditary spastic paraplegia false Inferred relationship Existential restriction modifier
Autosomal dominant spastic paraplegia type 17 Interprets Movement true Inferred relationship Existential restriction modifier 8
Autosomal dominant spastic paraplegia type 17 Finding site Structure of right lower limb true Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 17 Finding site Structure of left lower limb true Inferred relationship Existential restriction modifier 7
Autosomal dominant spastic paraplegia type 17 Interprets Movement observable true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 17 Has interpretation Absent true Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 17 Is a Autosomal dominant complex hereditary spastic paraplegia true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start