Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

Kleine-Levin Syndrome
Synonyms

familial Kleine-Levin syndrome

Kleine Levin syndrome

familial hibernation syndrome

Kleine-LEVIN hibernation syndrome

Kleine-Levin syndrome

Definitions

Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterized by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioral disturbances. A rare condition characterized by recurrent hypersomnias associated with hyperphagia, occurring primarily in males in the second to third decade of life. Clinical features include mental confusion, excessive sleep requirements (approximately 18 hours per day), restlessness, and in some cases hallucinations. Episodes have a duration of days to weeks, and may recur several times per year. This condition may resolve spontaneously over several years. (From Adams, et al., Principles of Neurology, 6th ed, p569)

ID

http://www.ebi.ac.uk/efo/EFO_1001354

database_cross_reference

NCIt:C84800

MESH:D017593

MONDO:0007863

MEDGEN:61511

icd11.foundation:1180849398

SCTID:111488004

MedDRA:10053712

DOID:0060165

MedDRA:10053742

Orphanet:33543

SNOMEDCT:111488004

ORDO:Orphanet_33543

OMIM:148840

MeSH:D017593

NCIT:C84800

UMLS:C0206085

DOID:60165

GARD:3117

NORD:1334

definition

Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterized by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioral disturbances.

A rare condition characterized by recurrent hypersomnias associated with hyperphagia, occurring primarily in males in the second to third decade of life. Clinical features include mental confusion, excessive sleep requirements (approximately 18 hours per day), restlessness, and in some cases hallucinations. Episodes have a duration of days to weeks, and may recur several times per year. This condition may resolve spontaneously over several years. (From Adams, et al., Principles of Neurology, 6th ed, p569)

gwas_trait

true

has_exact_synonym

Kleine-Levin syndrome

has_related_synonym

familial Kleine-Levin syndrome

Kleine Levin syndrome

familial hibernation syndrome

Kleine-LEVIN hibernation syndrome

id

EFO:1001354

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

Kleine-Levin Syndrome

notation

EFO:1001354

preferred label

Kleine-Levin Syndrome

prefLabel

Kleine-Levin Syndrome

see also

https://rarediseases.info.nih.gov/diseases/3117/kleine-levin-syndrome

skos_closeMatch

http://identifiers.org/meddra/10053712

skos_exactMatch

http://identifiers.org/snomedct/111488004

http://purl.obolibrary.org/obo/DOID_0060165

http://purl.obolibrary.org/obo/NCIT_C84800

http://identifiers.org/mesh/D017593

http://purl.obolibrary.org/obo/EFO_1001354

https://omim.org/entry/148840

http://linkedlifedata.com/resource/umls/id/C0206085

http://identifiers.org/medgen/61511

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1180849398

http://purl.obolibrary.org/obo/Orphanet_33543

term editor

Dani Welter

subClassOf

http://purl.obolibrary.org/obo/MONDO_0004617

http://www.ebi.ac.uk/efo/EFO_0005246

http://purl.obolibrary.org/obo/MONDO_0002254

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Delete Mapping To Ontology Source
http://www.ebi.ac.uk/efo/EFO_1001354 EFO SAME_URI
http://purl.bioontology.org/ontology/MEDDRA/10053742 MEDDRA LOOM
http://purl.obolibrary.org/obo/DOID_0060165 MFOMD LOOM
http://purl.obolibrary.org/obo/DOID_0060165 DTO LOOM
http://purl.obolibrary.org/obo/DOID_0060165 DOID LOOM
http://purl.obolibrary.org/obo/DOID_0060165 BAO LOOM
http://purl.obolibrary.org/obo/DOID_0060165 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0060165 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_0060165 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0060165 FNS-H LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#20802 OCHV LOOM
http://purl.obolibrary.org/obo/NCIT_C84800 BERO LOOM
http://purl.obolibrary.org/obo/MONDO_0007863 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0007863 DOVES LOOM
http://purl.bioontology.org/ontology/MESH/D017593 MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_10326 HRDO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84800 NCIT LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Kleine_Levin_Syndrome APADISORDERS LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Kleine_Levin_Syndrome APAONTO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Kleine-Levin_Syndrome CSEO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.886.425.800.200.500 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/D9-74270 SNMI LOOM
http://purl.jp/bio/4/id/200906062726138119 IOBC LOOM
http://purl.bioontology.org/ontology/RCTV2/Fy06.00 RCTV2 LOOM
http://www.ebi.ac.uk/efo/EFO_1001354 EFO LOOM
http://purl.obolibrary.org/obo/OMIT_0017926 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#F03.870.400.800.200.500 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0206085 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D017593 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/111488004 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/RCD/X008E RCD LOOM
http://www.orpha.net/ORDO/Orphanet_33543 ORDO LOOM