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763803004: Morvan syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3644052014 Morvan syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3644053016 Morvan syndrome en Synonym Active Case sensitive SNOMED CT core
3644055011 Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome en Synonym Active Case insensitive SNOMED CT core
3644056012 Morvan fibrillary chorea en Synonym Active Case sensitive SNOMED CT core
3644054010 A rare life threatening acquired neurologic disease with characteristics of neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Morvan syndrome Interprets Movement true Inferred relationship Some 3
Morvan syndrome Is a Movement disorder true Inferred relationship Some
Morvan syndrome Is a Encephalopathy true Inferred relationship Some
Morvan syndrome Is a Peripheral neuropathy true Inferred relationship Some
Morvan syndrome Finding site Brain structure true Inferred relationship Some 1
Morvan syndrome Finding site Peripheral nerve structure 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

Description inactivation indicator reference set

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