OPRM1, opioid receptor mu 1, 4988

N. diseases: 370; N. variants: 42
Disease: Seizures ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures 		0.310 GeneticVariation phenotype BEFREE The OPRM1 (rs1799971) polymorphism was investigated in an association study of a group of ADS patients (n = 177) and in subgroups (delirium tremens and/or seizures, age at onset <26 years, dissocial alcoholics, positive familial history of alcoholism, delirium tremens, and seizures). 30085428 2019
CUI: C0036572
Disease: Seizures
Seizures 		0.310 Biomarker phenotype CTD_human Mechanisms of morphine enhancement of spontaneous seizure activity. 18042875 2007
CUI: C0036572
Disease: Seizures
Seizures 		0.310 Biomarker phenotype CTD_human [The role of the opiate mechanisms of the hippocampus and substantia nigra in the behavioral and convulsive disorders in picrotoxin-induced kindling]. 1675896 1991