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narcolepsy 7

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any narcolepsy in which the cause of the disease is a mutation in the MOG gene.
Uniprot Description Neurological disabling sleep disorder, characterized by excessive daytime sleepiness, sleep fragmentation, symptoms of abnormal rapid-eye-movement (REM) sleep, cataplexy, hypnagogic hallucinations, and sleep paralysis. Cataplexy is a sudden loss of muscle tone triggered by emotions, which is the most valuable clinical feature used to diagnose narcolepsy. Human narcolepsy is primarily a sporadically occurring disorder but familial clustering has been observed.
Mondo Term and Equivalent IDs
MONDO:0013652:  narcolepsy 7
UMLS:C3280266: