Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225318
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
0.600 GeneticVariation disease UNIPROT Galanin pathogenic mutations in temporal lobe epilepsy. 25691535 2015
CUI: C4225318
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
0.600 Biomarker disease GENOMICS_ENGLAND Galanin pathogenic mutations in temporal lobe epilepsy. 25691535 2015
CUI: C4225318
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
EPILEPSY, FAMILIAL TEMPORAL LOBE, 8
0.600 Biomarker disease CTD_human