DisGeNET - a database of gene-disease associations

Source: ALL

Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR ×

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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:	3146
Gene Symbol:	HMGB1

HMGB1

CUI:	C1846385
Disease:	FOCAL CORTICAL DYSPLASIA OF TAYLOR

FOCAL CORTICAL DYSPLASIA OF TAYLOR

0.010

AlteredExpression

BEFREE

Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II.

2018