Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757129010 | Pharyngo-cervico-brachial variant of Guillain-Barré syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3757130017 | Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3757131018 | Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3777265011 | PCB (pharyngeal-cervical-brachial) variant of Guillain-Barré syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3757133015 | A rare acquired peripheral neuropathy disease with characteristics of progressive oropharyngeal (facial palsy, dysarthria) and cervicobrachial weakness, associated with upper limb weakness and hypo/areflexia in the absence of ophthalmoplegia, ataxia, altered consciousness, and prominent lower limb weakness. The presence of monospecific IgG anti-GT1a antibodies is associated. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Is a | Guillain-Barré syndrome | true | Inferred relationship | Some | ||
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Associated morphology | Demyelination | true | Inferred relationship | Some | 2 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Clinical course | Sudden onset AND/OR short duration (qualifier value) | true | Inferred relationship | Some | 3 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 2 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Finding site | Nerve structure | false | Inferred relationship | Some | 1 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Associated morphology | Inflammation | false | Inferred relationship | Some | 1 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 1 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 2 | |
Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets