DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Congenital neurologic anomalies ×

Results per page

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:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C0497552
Disease:	Congenital neurologic anomalies

Congenital neurologic anomalies

0.010

Biomarker

BEFREE

Central nervous system malformations and deformations in FGFR2-related craniosynostosis.

2012