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1187468005: Autosomal dominant spastic paraplegia type 73 (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
4673893013 Autosomal dominant spastic paraplegia type 73 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673894019 Autosomal dominant spastic paraplegia type 73 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4673895018 A pure form of hereditary spastic paraplegia with characteristics of adult onset of crural spastic paraparesis, hyperreflexia, extensor plantar responses, proximal muscle weakness, mild muscle atrophy, decreased vibration sensation at ankles and mild urinary dysfunction. Foot deformities have been reported to eventually occur in some patients. No abnormalities are noted on brain magnetic resonance imaging and peripheral nerve conduction velocity studies. 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 73 est un(e) (attribut) Pure hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 73 est un(e) (attribut) Autosomal dominant hereditary spastic paraplegia true Inferred relationship Some
Autosomal dominant spastic paraplegia type 73 évolution clinique (attribut) progressif true Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 73 localisation d'une constatation (attribut) membre inférieur true Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 73 localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 73 morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada French language reference set (foundation metadata concept)

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