DisGeNET - a database of gene-disease associations

Source: INFERRED

Disease: Mesial temporal lobe epilepsy with hippocampal sclerosis ×

Gene: SCN1A ×

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	6323
Gene Symbol:	SCN1A

SCN1A

CUI:	C4749367
Disease:	Mesial temporal lobe epilepsy with hippocampal sclerosis

Mesial temporal lobe epilepsy with hippocampal sclerosis

0.110

GeneticVariation

GWASCAT

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

24014518

2013

Entrez Id:	6323
Gene Symbol:	SCN1A