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 2 1.1E-02 0 0
CUI: C0043515
Disease: Zollinger-Ellison syndrome
Zollinger-Ellison syndrome 		20 0 1 7.9E-03 0 0
CUI: C0796013
Disease: Zimmerman Laband syndrome
Zimmerman Laband syndrome 		8 0 1 8.7E-03 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 3 1.0E-02 0 0
CUI: C4310696
Disease: Zhu-Tokita-Takenouchi-Kim syndrome
Zhu-Tokita-Takenouchi-Kim syndrome 		1 0 1 9.3E-03 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome 		13 0 1 8.3E-03 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 1 7.0E-03 0 0
CUI: C4687396
Disease: Zellweger Spectrum Disorder
Zellweger Spectrum Disorder 		6 0 1 8.8E-03 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 7.8E-03 0 0
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME 		1 0 1 9.3E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 1 5.7E-03 0 0
CUI: C1863008
Disease: Yellow-brown discoloration of the teeth
Yellow-brown discoloration of the teeth 		7 0 1 8.8E-03 0 0
CUI: C4750849
Disease: XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation
XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation 		1 0 1 9.3E-03 0 0
CUI: C0432475
Disease: XX males
XX males 		32 0 1 7.2E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 1 6.1E-03 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 1 5.7E-03 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 2 8.2E-03 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 1 7.9E-03 0 0
CUI: C0549463
Disease: X-Linked Lymphoproliferative Disorder
X-Linked Lymphoproliferative Disorder 		49 0 1 6.4E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 6.3E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 7 4.2E-02 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 1 6.1E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 5 1.8E-02 0 0
CUI: C0406587
Disease: Wrinkly skin syndrome
Wrinkly skin syndrome 		3 0 1 9.1E-03 0 0
CUI: C3280358
Disease: Wolfram-Like Syndrome, Autosomal Dominant
Wolfram-Like Syndrome, Autosomal Dominant 		1 0 1 9.3E-03 0 0