MOG, myelin oligodendrocyte glycoprotein, 4340

N. diseases: 136; N. variants: 10
Disease: Narcolepsy-Cataplexy Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome 		0.510 SusceptibilityMutation disease ORPHANET A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome 		0.510 GeneticVariation disease BEFREE A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome 		0.510 Biomarker disease CTD_human