DisGeNET - a database of gene-disease associations

Gene: FGFR2 ×

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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:	2263
Gene Symbol:	FGFR2

FGFR2

CUI:	C1867564
Disease:	SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY

SCAPHOCEPHALY AND AXENFELD-RIEGER ANOMALY

0.400

Biomarker

GENOMICS_ENGLAND

Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.

2016