Narcolepsy 7 - CISMeF

Preferred Label : Narcolepsy 7;

Symbol : NRCLP7;

CISMeF acronym : NRCLP7;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the myelin-oligodendrocyte glycoprotein (MOG, 159465.0001);

Laboratory abnormalities : Decreased levels of CSF hypocretin (HCRT, 602358);

Prefixed ID : #614250;

Details

Origin ID

614250;

UMLS CUI

C3280266;

Automatic exact mappings (from CISMeF team)
- Narcolepsy type 1 [ORDO Disease]
DO Cross reference
- narcolepsy [DO Concept]
Genes related to phenotype
- Myelin-oligodendrocyte glycoprotein [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Cataplexy [HPO term]
- Excessive daytime sleepiness [HPO term]
- Excessive daytime somnolence [HPO term]
- Narcolepsy [HPO term]
- Obesity [HPO term]
- Type II diabetes mellitus [HPO term]
ORDO concept(s)
- Narcolepsy type 1 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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