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: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 0 7 1.9E-02 0 0
CUI: C0043541
Disease: Zygomycosis
Zygomycosis 		9 0 2 6.5E-03 0 0
CUI: C0276883
Disease: Zoonotic form of cutaneous leishmaniasis
Zoonotic form of cutaneous leishmaniasis 		6 0 1 3.2E-03 0 0
CUI: C0043528
Disease: Zoonoses
Zoonoses 		19 0 2 6.3E-03 0 0
CUI: C0043515
Disease: Zollinger-Ellison syndrome
Zollinger-Ellison syndrome 		20 0 6 1.9E-02 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 6 1.6E-02 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 13 2.7E-02 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 2 5.9E-03 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 3.1E-03 0 0
CUI: C1863557
Disease: Young Simpson syndrome
Young Simpson syndrome 		2 0 1 3.3E-03 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 2.8E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 8 2.2E-02 0 0
CUI: C0043407
Disease: Yersinia infections
Yersinia infections 		17 0 1 3.1E-03 0 0
CUI: C1866425
Disease: Yemenite deaf-blind hypopigmentation syndrome
Yemenite deaf-blind hypopigmentation syndrome 		1 0 1 3.3E-03 0 0
CUI: C1850533
Disease: Yellow subcutaneous tissue covered by thin, scaly skin
Yellow subcutaneous tissue covered by thin, scaly skin 		1 0 1 3.3E-03 0 0
CUI: C0043395
Disease: Yellow Fever
Yellow Fever 		28 0 4 1.2E-02 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 3.3E-03 0 0
CUI: C4020788
Disease: Xy female gonadal dysgenesis
Xy female gonadal dysgenesis 		1 0 1 3.3E-03 0 0
CUI: C0432475
Disease: XX males
XX males 		32 0 4 1.2E-02 0 0
CUI: C1970416
Disease: XFE Progeroid Syndrome
XFE Progeroid Syndrome 		3 0 1 3.3E-03 0 0
CUI: C0259817
Disease: Xerosis
Xerosis 		4 0 1 3.3E-03 0 0
CUI: C3806565
Disease: XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME
XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME 		1 0 1 3.3E-03 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 3 9.4E-03 0 0
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		8 31 1 3.2E-03 2 3.8E-02
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 2 6.4E-03 0 0