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 		0.300 GermlineCausalMutation disease ORPHANET Mutations in DEPDC5 cause familial focal epilepsy with variable foci. 23542697 2013
CUI: C1838062
Disease: Autosomal Dominant Lateral Temporal Lobe Epilepsy
Autosomal Dominant Lateral Temporal Lobe Epilepsy 		0.300 GermlineCausalMutation disease ORPHANET Mutations of DEPDC5 cause autosomal dominant focal epilepsies. 23542701 2013