DisGeNET - a database of gene-disease associations

Source: RGD

Disease: HELLP Syndrome ×

Gene: FASLG ×

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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:	356
Gene Symbol:	FASLG

FASLG

CUI:	C0162739
Disease:	HELLP Syndrome

HELLP Syndrome

0.220

Biomarker

RGD

Dysregulation of the Fas/FasL system in an experimental animal model of HELLP syndrome.

2017