cataplexy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A sudden and transient episode of bilateral loss of muscle tone, often triggered by emotions. (Human Phenotype Ontology, HP_0002524)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002524
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Genes

5 genes associated with the cataplexy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DNMT1 DNA (cytosine-5-)-methyltransferase 1
HCRT hypocretin (orexin) neuropeptide precursor
MOG myelin oligodendrocyte glycoprotein
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2