RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: Epilepsy, Familial Temporal Lobe 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
Epilepsy, Familial Temporal Lobe 1 		0.310 GeneticVariation disease BEFREE The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations. 28142128 2017
CUI: C4551957
Disease: Epilepsy, Familial Temporal Lobe 1
Epilepsy, Familial Temporal Lobe 1 		0.310 Biomarker disease CTD_human