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766722008: Paraparetic variant of Guillain-Barré syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3662393016 Paraparetic variant of Guillain-Barré syndrome en Synonym Active Initial character case insensitive SNOMED CT core
3662394010 Paraparetic variant of Guillain-Barré syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3662392014 A rare variant of Guillain-Barre syndrome with characteristics of isolated leg weakness, areflexia and radicular leg pain that may simulate a cauda equina or spinal cord syndrome. The arms, ocular, facial, and oropharyngeal muscles are spared and sphincteric function is normal. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Paraparetic variant of Guillain-Barré syndrome Associated morphology Inflammatory morphology true Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome Finding site Peripheral nerve structure true Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome Pathological process Autoimmune process true Inferred relationship Some 2
Paraparetic variant of Guillain-Barré syndrome Pathological process Autoimmune process true Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome Is a Guillain-Barré syndrome true Inferred relationship Some
Paraparetic variant of Guillain-Barré syndrome Clinical course Acute true Inferred relationship Some 3
Paraparetic variant of Guillain-Barré syndrome Finding site Nerve structure false Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome Associated morphology Inflammation false Inferred relationship Some 1
Paraparetic variant of Guillain-Barré syndrome Finding site Peripheral nerve structure true Inferred relationship Some 2
Paraparetic variant of Guillain-Barré syndrome Associated morphology Demyelination true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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