DisGeNET - a database of gene-disease associations

Source: INFERRED

Disease: Night blindness, congenital stationary ×

Gene: NYX ×

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:	60506
Gene Symbol:	NYX

NYX

CUI:	C0339535
Disease:	Night blindness, congenital stationary

Night blindness, congenital stationary

0.700

Biomarker

HPO

Entrez Id:	60506
Gene Symbol:	NYX

NYX

CUI:	C0339535
Disease:	Night blindness, congenital stationary

Night blindness, congenital stationary

0.700

GeneticVariation

CLINVAR