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716722005: acute motorische en sensorische axonale neuropathie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307322013 Acute motor sensory axonal Guillain-Barré syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307323015 Acute motor sensory axonal neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312528010 Acute motor sensory axonal Guillain-Barré syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
8187671000146117 acute motorische en sensorische axonale neuropathie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8187681000146115 acute motorische en sensorische axonale neuropathie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8187691000146118 acute motorische en sensorische axonale vorm van guillain-barrésyndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8188071000146114 acute motorisch en sensorische axonale vorm van syndroom van Guillain-Barré nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3307325010 A motor sensory axonal form of Guillain-Barré syndrome. Patients present with muscle weakness and sensory deficits, similar to that of the more frequent demyelinating form of Guillain-Barré syndrome. As in other types of Guillain-Barré syndrome, an infectious disease precedes the onset of limb weakness in the majority of cases. Although the exact pathological mechanism is poorly understood the disease is associated with the presence of antiganglioside antibodies and may be caused by antibody-mediated primary axonal degeneration or antibody-mediated inhibition of voltage-gated sodium channels. 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
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Is a Guillain-Barré syndrome true Inferred relationship Some
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Clinical course Sudden onset AND/OR short duration (qualifier value) true Inferred relationship Some 1
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Associated morphology Demyelination true Inferred relationship Some 3
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Finding site Peripheral nerve structure true Inferred relationship Some 3
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Associated morphology ontsteking (afwijkende morfologie) false Inferred relationship Some 4
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Finding site Nerve structure false Inferred relationship Some 4
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Finding site Peripheral nerve structure true Inferred relationship Some 2
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 2
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 3
Acute motor sensory axonal Guillain-Barré syndrome (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Dutch rare neuromuscular disorders simple reference set (foundation metadata concept)

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