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: C0271987
Disease: ^A^gamma delta beta^0^ thalassemia
^A^gamma delta beta^0^ thalassemia 		4 0 1 3.7E-03 0 0
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		69 23 2 6.0E-03 1 6.7E-04
CUI: C0043541
Disease: Zygomycosis
Zygomycosis 		9 0 1 3.7E-03 0 0
CUI: C0043515
Disease: Zollinger-Ellison syndrome
Zollinger-Ellison syndrome 		20 0 1 3.5E-03 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 1 2.8E-03 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 2 4.4E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 1 3.0E-03 0 0
CUI: C0043407
Disease: Yersinia infections
Yersinia infections 		17 0 1 3.6E-03 0 0
CUI: C2609184
Disease: Yellow fever vaccine-associated viscerotropic disease
Yellow fever vaccine-associated viscerotropic disease 		2 0 1 3.8E-03 0 0
CUI: C0750466
Disease: Yeast infection
Yeast infection 		2 0 1 3.8E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 2 6.3E-03 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 1 3.2E-03 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 1 3.0E-03 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 2 6.0E-03 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 1 2.5E-03 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 2 6.6E-03 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 2 7.1E-03 0 0
CUI: C1337035
Disease: Xanthogranulomatous cholecystitis
Xanthogranulomatous cholecystitis 		6 0 1 3.7E-03 0 0
CUI: C4304338
Disease: X-linked sideroblastic anemia with spinocerebellar ataxia
X-linked sideroblastic anemia with spinocerebellar ataxia 		1 0 1 3.8E-03 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 1 3.6E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 3.2E-03 0 0
CUI: C0751337
Disease: X-Linked Emery-Dreifuss Muscular Dystrophy
X-Linked Emery-Dreifuss Muscular Dystrophy 		20 0 1 3.5E-03 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 1 3.1E-03 0 0
CUI: C4016809
Disease: WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET
WOLFF-PARKINSON-WHITE SYNDROME, CHILDHOOD-ONSET 		1 0 1 3.8E-03 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 3 9.7E-03 0 0