MGMT, O-6-methylguanine-DNA methyltransferase, 4255

N. diseases: 444; N. variants: 24
Disease: Early infantile epileptic encephalopathy with suppression bursts ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0393706
Disease: Early infantile epileptic encephalopathy with suppression bursts
Early infantile epileptic encephalopathy with suppression bursts 		0.010 PosttranslationalModification disease BEFREE RPA VI (p = 0.048) and absence of MGMT methylation (p = 0.001) worsened OS significantly. 31054101 2019