You are using an outdated browser. Please upgrade your browser to improve your experience.
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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:614250
UMLS:C3280266
MONDO:0013652
High level summary of knowledge for a disease, including descriptions and datasource references.