Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		176 0 1 5.3E-03 0 0
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		378 0 1 2.6E-03 0 0
CUI: C0948441
Disease: Venoocclusive disease
Venoocclusive disease 		34 0 1 2.2E-02 0 0
CUI: C0947751
Disease: Vascular inflammations
Vascular inflammations 		305 0 1 3.2E-03 0 0
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		688 0 1 1.4E-03 0 0
CUI: C0342649
Disease: Vascular calcification
Vascular calcification 		257 0 1 3.7E-03 0 0
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria 		21 0 1 3.0E-02 0 0
CUI: C0042345
Disease: Varicosity
Varicosity 		188 0 1 5.0E-03 0 0
CUI: C0042344
Disease: Varicose Ulcer
Varicose Ulcer 		38 0 1 2.0E-02 0 0
CUI: C0042267
Disease: Vaginitis
Vaginitis 		12 0 1 4.2E-02 0 0
CUI: C0041948
Disease: Uremia
Uremia 		110 0 1 8.2E-03 0 0
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		235 0 1 4.0E-03 0 0
CUI: C4725093
Disease: Unresectable Melanoma
Unresectable Melanoma 		7 0 1 5.3E-02 0 0
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		17 0 1 3.4E-02 0 0
CUI: C0268623
Disease: Tyrosinemia, Type III
Tyrosinemia, Type III 		4 0 1 6.2E-02 0 0
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I 		18 0 1 3.3E-02 0 0
CUI: C0268487
Disease: Tyrosine Transaminase Deficiency Disease
Tyrosine Transaminase Deficiency Disease 		7 0 1 5.3E-02 0 0
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		6626 0 2 3.0E-04 0 0
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis 		328 0 1 2.9E-03 0 0
CUI: C0041341
Disease: Tuberous Sclerosis
Tuberous Sclerosis 		289 0 1 3.3E-03 0 0
CUI: C0041323
Disease: Tuberculosis, Oral
Tuberculosis, Oral 		2 0 1 7.1E-02 0 0
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		1256 0 2 1.6E-03 0 0
CUI: C0268238
Disease: Triglyceride storage disease with ichthyosis
Triglyceride storage disease with ichthyosis 		41 0 3 5.9E-02 0 0
CUI: C3714237
Disease: Trifunctional Protein Deficiency, Type 2
Trifunctional Protein Deficiency, Type 2 		2 0 2 0.15 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 3 9.1E-02 0 0