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Orphanet Rare Disease Ontology
Last uploaded:
December 4, 2024
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| Preferred Name | Kleine-Levin syndrome | |
| Synonyms |
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| Definitions |
Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterised by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioural disturbances. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_33543 |
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| definition |
Kleine-Levin syndrome (KLS) is a rare neurological disorder of unknown origin characterised by relapsing-remitting episodes of hypersomnia in association with cognitive and behavioural disturbances.
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| definition_citation |
Orphanet
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=33543 |
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| has_age_of_onset |
Adolescent Adult Childhood
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| hasDbXref |
ICD-11:7A22 ICD-10:G47.8 MedDRA:10053712 OMIM:148840 MeSH:D017593 UMLS:C0206085
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| label |
Kleine-Levin syndrome
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| notation |
ORPHA:33543
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_33543
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| prefLabel |
Kleine-Levin syndrome
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| present_in |
France AND has_point_prevalence_average_value : 0.18 AND has_point_prevalence_range : 1-9 / 1 000 000 Europe AND has_point_prevalence_range : 1-9 / 1 000 000
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