Kleine-levin hibernation syndrome

Preferred Label : Kleine-levin hibernation syndrome;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Kleine-levin syndrome;

Description : The Kleine-Levin hibernation syndrome is a rare disorder that occurs predominantly in males and is characterized by episodic attacks of aberrant behavior, hypersomnia, and increased feeding (megaphagia) and sex drives (Kleine, 1925; Levin, 1929).;

Inheritance : Autosomal dominant;

Prefixed ID : %148840;

Details

Origin ID

148840;

UMLS CUI

C0206085;

Automatic exact mappings (from CISMeF team)
- Other sleep disorders [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Hypersomnia-bulimia syndrome [MedDRA Preferred Term]
- Kleine Levin syndrome [Disease (Nov.)]
- Kleine-Levin Syndrome [NCIt concept]
- Kleine-Levin syndrome [PASCAL descriptor]
- Kleine-Levin syndrome [DO Concept]
- Kleine-Levin syndrome [ICD-11 Category]
- Kleine-Levin syndrome [MeSH concept]
- Kleine-Levin syndrome [ORDO Disease]
- Kleine-Levin syndrome [MedDRA LLT]
- Kleine-Levin syndrome (disorder) [SNOMED CT concept]
- kleine-levin syndrome [MeSH Descriptor]
- kleine-levin syndrome [SNOMED Notion]
DO Cross reference
- Kleine-Levin syndrome [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Confusion [HPO term]
- Episodic hypersomnia [HPO term]
- Hyperphagia [HPO term]
- Polyphagia [HPO term]
- Vivid hallucinations [HPO term]
ORDO concept(s)
- Kleine-Levin syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypersomnia-bulimia syndrome [MedDRA Preferred Term]
- Kleine Levin syndrome [Disease (Nov.)]
- Kleine-Levin Syndrome [NCIt concept]
- Kleine-Levin syndrome [MedDRA LLT]
- Kleine-Levin syndrome [ORDO Disease]
- Kleine-Levin syndrome [MeSH concept]
- Kleine-Levin syndrome [DO Concept]
- Kleine-Levin syndrome [PASCAL descriptor]
- Kleine-Levin syndrome (disorder) [SNOMED CT concept]
- kleine-levin syndrome [SNOMED Notion]
- kleine-levin syndrome [MeSH Descriptor]

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