RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Lateral Temporal Lobe Epilepsy 		0.310 GeneticVariation disease BEFREE Heterozygous RELN mutations cause a typical ADLTE syndrome, indistinguishable from that associated with LGI1 mutations. 28142128 2017
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Lateral Temporal Lobe Epilepsy 		0.310 GermlineCausalMutation disease ORPHANET Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. 26046367 2015