Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 GeneticVariation UNIPROT WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation. 25411445

2015
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 Biomarker GENOMICS_ENGLAND The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration. 24456803

2014
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 Biomarker GENOMICS_ENGLAND The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration. 24456803

2014
Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 Biomarker CTD_human

Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 CausalMutation CLINVAR

Entrez Id: 51741
Gene Symbol: WWOX
WWOX
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 GeneticVariation CLINVAR