RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		0.700 GeneticVariation disease UNIPROT Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. 26046367 2015
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		0.700 Biomarker disease GENOMICS_ENGLAND Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. 26046367 2015
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		0.700 CausalMutation disease CLINVAR
CUI: C4225327
Disease: EPILEPSY, FAMILIAL TEMPORAL LOBE, 7
EPILEPSY, FAMILIAL TEMPORAL LOBE, 7 		0.700 Biomarker disease CTD_human