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1172701002: faciale diplegie met paresthesie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4635456018 Facial diplegia with paresthesia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4635457010 Facial diplegia with paresthesia variant of Guillain-Barré syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4635458017 Facial diplegia with paraesthesia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4635459013 Facial diplegia with paraesthesia variant of Guillain-Barré syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4635460015 Facial diplegia with paresthesia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13123241000146111 faciale diplegie met paresthesie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13123251000146114 diplegia facialis met paresthesie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13123261000146112 faciale diplegie met paresthesie-variant van Guillain-Barré-syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13123271000146118 faciale diplegie met paresthesie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4635461016 A rare localised variant of Guillain-Barré syndrome characterised by rapidly progressive bilateral facial nerve palsy, distal paraesthesia and minimal or no motor weakness. Deep tendon reflexes are usually diminished or absent but can be present or even exaggerated in rare cases. Cerebrospinal fluid analysis may reveal albuminocytologic dissociation. Nerve conduction velocity studies often show demyelinating type of neuropathy although axonal polyneuropathy has been also described. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4635462011 A rare localized variant of Guillain-Barré syndrome characterized by rapidly progressive bilateral facial nerve palsy, distal paresthesia and minimal or no motor weakness. Deep tendon reflexes are usually diminished or absent but can be present or even exaggerated in rare cases. Cerebrospinal fluid analysis may reveal albuminocytologic dissociation. Nerve conduction velocity studies often show demyelinating type of neuropathy although axonal polyneuropathy has been also described. 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
Facial diplegia with paresthesia (disorder) Is a Facial palsy true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Guillain-Barré syndrome true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Cranial neuritis true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Paresthesia true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Clinical course Sudden onset AND/OR short duration (qualifier value) true Inferred relationship Some 4
Facial diplegia with paresthesia (disorder) Interprets Movement true Inferred relationship Some 5
Facial diplegia with paresthesia (disorder) Interprets Gross movement of body and limbs true Inferred relationship Some 3
Facial diplegia with paresthesia (disorder) Has interpretation Absent true Inferred relationship Some 3
Facial diplegia with paresthesia (disorder) Finding site Facial nerve structure true Inferred relationship Some 1
Facial diplegia with paresthesia (disorder) Associated morphology Demyelination true Inferred relationship Some 1
Facial diplegia with paresthesia (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 1
Facial diplegia with paresthesia (disorder) Finding site Facial nerve structure true Inferred relationship Some 2
Facial diplegia with paresthesia (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 2
Facial diplegia with paresthesia (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 2
Facial diplegia with paresthesia (disorder) Is a Gross movement of body and limbs - finding true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Nerve palsy true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Autoimmune movement disorder true Inferred relationship Some
Facial diplegia with paresthesia (disorder) Is a Loss of motor function true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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