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1187466009: Autosomal dominant spastic paraplegia type 9B (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4673887017 Autosomal dominant spastic paraplegia type 9B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4673888010 Autosomal dominant spastic paraplegia type 9B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5399622010 A rare predominantly pure hereditary spastic paraplegia characterized by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399623017 A rare predominantly pure hereditary spastic paraplegia characterised by juvenile or adult onset of slowly progressive spastic paraparesis, gait disturbances, and increased tendon reflexes. Additional variable manifestations include pes cavus, dysarthria, sensory impairment, and urinary symptoms. Cognition is normal. 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 9B Is a Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 9B Clinical course Progressive (qualifier value) true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 9B Finding site Lower limb structure false Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9B Finding site Spinal cord structure true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 9B Associated morphology Degenerative abnormality true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 9B Interprets Movement true Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 9B Finding site Structure of right lower limb (body structure) true Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 9B Finding site Structure of left lower limb (body structure) true Inferred relationship Some 5
Autosomal dominant spastic paraplegia type 9B Interprets Movement observable true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9B Has interpretation Absent true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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