Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206085
Disease: Kleine-Levin Syndrome
Kleine-Levin Syndrome
0.320 Biomarker disease GENOMICS_ENGLAND Familial Kleine-Levin Syndrome: A Specific Entity? 27253765 2016
CUI: C0206085
Disease: Kleine-Levin Syndrome
Kleine-Levin Syndrome
0.320 Biomarker disease GENOMICS_ENGLAND An association analysis of HLA-DQB1 with narcolepsy without cataplexy and idiopathic hypersomnia with/without long sleep time in a Japanese population. 27081540 2015
CUI: C0206085
Disease: Kleine-Levin Syndrome
Kleine-Levin Syndrome
0.320 Biomarker disease BEFREE We report that an immunoresponsive HLA-DQB1, DQB1∗0602, was detected in significant quantities in patients with KLS (three of 12, p=0.046) and could elevate the risk of KLS (odds ratio, 1.143; 95% confidence interval, 0.0982-1.329). 22285112 2012
CUI: C0206085
Disease: Kleine-Levin Syndrome
Kleine-Levin Syndrome
0.320 GeneticVariation disease BEFREE The authors collected clinical, polysomnographic, CSF, CT, and MRI records and analyzed gene polymorphisms of HLA-DQB1, tryptophan hydroxylase (TpH), and catechol-O-methyltransferase (COMT) in 30 unrelated patients with KLS and their families. 12473762 2002