DisGeNET - a database of gene-disease associations

Gene: WWOX ×

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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:	51741
Gene Symbol:	WWOX

WWOX

CUI:	C4510744
Disease:	46,XY partial gonadal dysgenesis

46,XY partial gonadal dysgenesis

0.300

GermlineCausalMutation

ORPHANET

A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development.

2012