WWOX, WW domain containing oxidoreductase, 51741

N. diseases: 356; N. variants: 58
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280452
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12 		0.730 Biomarker disease GENOMICS_ENGLAND
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 Biomarker disease CTD_human
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 CausalMutation disease CLINVAR
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		0.700 GeneticVariation disease CLINVAR
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.610 CausalMutation disease CLINVAR
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.610 Biomarker disease CTD_human
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.610 CausalMutation disease CGI
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.600 CausalMutation group CGI
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.600 Biomarker group CTD_human
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.460 Biomarker disease HPO
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.410 Biomarker disease HPO
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.410 CausalMutation disease CGI
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		0.320 Biomarker disease CTD_human
CUI: C0153942
Disease: Benign neoplasm of esophagus
Benign neoplasm of esophagus 		0.300 CausalMutation disease CGI
CUI: C0154059
Disease: Carcinoma in situ of esophagus
Carcinoma in situ of esophagus 		0.300 CausalMutation disease CGI
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		0.300 Biomarker disease CTD_human
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		0.300 Biomarker disease CTD_human
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		0.300 Biomarker disease CTD_human
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		0.300 Biomarker disease CTD_human
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		0.300 Biomarker disease CTD_human
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		0.300 Biomarker disease CTD_human
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.170 Biomarker disease HPO
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.170 GeneticVariation disease CLINVAR
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		0.140 Biomarker group HPO
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.130 Biomarker disease HPO