DisGeNET - a database of gene-disease associations

Congenital absence of kidneys syndrome, C1609433

Gene: FGF20 ×

Source: ALL

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

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	26281
Gene Symbol:	FGF20

FGF20

0.400

GermlineCausalMutation

disease

ORPHANET

FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.

2012

Entrez Id:	26281
Gene Symbol:	FGF20

FGF20

0.400

Biomarker

disease

HPO