Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

Morvan syndrome
Synonyms

Morvan's fibrillary chorea

Morvan's syndrome

limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome

Morvan syndrome

MFC

MoS

Definitions

Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by 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. Morvan syndrome is a rare autoimmune/paraneoplastic disorder involving antibodies to the voltage-gated potassium channel complex. It is defined by subacute encephalopathy, neuromuscular hyperexcitability, dysautonomia, and sleep disturbance. [PMID:27224435]

ID

http://www.ebi.ac.uk/efo/EFO_1001897

database_cross_reference

Orphanet:83467

MONDO:0008718

ORDO:Orphanet_83467

MedDRA:10075006

SCTID:763803004

MEDGEN:1632829

UMLS:C3854373

Wikipedia:Morvan%27s_syndrome

GARD:9766

definition

Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by 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.

Morvan syndrome is a rare autoimmune/paraneoplastic disorder involving antibodies to the voltage-gated potassium channel complex. It is defined by subacute encephalopathy, neuromuscular hyperexcitability, dysautonomia, and sleep disturbance. [PMID:27224435]

has_exact_synonym

Morvan's fibrillary chorea

Morvan's syndrome

limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome

Morvan syndrome

MFC

MoS

id

EFO:1001897

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder

label

Morvan syndrome

notation

EFO:1001897

preferred label

Morvan syndrome

prefLabel

Morvan syndrome

skos_exactMatch

http://purl.obolibrary.org/obo/Orphanet_83467

http://identifiers.org/medgen/1632829

http://identifiers.org/snomedct/763803004

http://purl.obolibrary.org/obo/EFO_1001897

http://linkedlifedata.com/resource/umls/id/C3854373

term editor

Gautier Koscielny

subClassOf

http://www.ebi.ac.uk/efo/EFO_1001899

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