Details of Disease | DrugMAP

General Information of Disease (ID: DISC8XN6)

Disease Name	Narcolepsy 7
Synonyms	NRCLP7; narcolepsy caused by mutation in MOG; narcolepsy 7; narcolepsy type 7; MOG narcolepsy
Definition	Any narcolepsy in which the cause of the disease is a mutation in the MOG gene.
Disease Hierarchy	DISLCNLI: Narcolepsy DIS4RKXT: Hereditary narcolepsy DISH7Y6Q: Narcolepsy type 1 DISC8XN6: Narcolepsy 7
Disease Identifiers	MONDO ID MONDO_0013652 UMLS CUI C3280266 OMIM ID 614250 MedGen ID 481896

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 2 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
MOG	TTQAFX5	Limited	Unknown	[1]
MOG	TTQAFX5	moderate	Biomarker	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MOG	OTYNB7Y5	Limited	Unknown	[1]
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References

1	A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. Am J Hum Genet. 2011 Sep 9;89(3):474-9. doi: 10.1016/j.ajhg.2011.08.007.