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 1.4E-02 0 0
CUI: C0043541
Disease: Zygomycosis
Zygomycosis 		9 0 1 1.1E-02 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 1 6.0E-03 0 0
CUI: C4225321
Disease: ZIMMERMANN-LABAND SYNDROME 2
ZIMMERMANN-LABAND SYNDROME 2 		1 0 1 1.3E-02 0 0
CUI: C4551773
Disease: ZIMMERMANN-LABAND SYNDROME 1
ZIMMERMANN-LABAND SYNDROME 1 		2 0 1 1.3E-02 0 0
CUI: C0796013
Disease: Zimmerman Laband syndrome
Zimmerman Laband syndrome 		8 0 1 1.2E-02 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 2 7.4E-03 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 7.8E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 2 1.4E-02 0 0
CUI: C1866425
Disease: Yemenite deaf-blind hypopigmentation syndrome
Yemenite deaf-blind hypopigmentation syndrome 		1 0 1 1.3E-02 0 0
CUI: C4525234
Disease: Xiphophorus Melanoma
Xiphophorus Melanoma 		2 0 1 1.3E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 1 7.5E-03 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 1 6.8E-03 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 1 6.8E-03 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 1 9.3E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 3 2.3E-02 0 0
CUI: C4551551
Disease: X-linked hereditary motor and sensory neuropathy
X-linked hereditary motor and sensory neuropathy 		7 0 1 1.2E-02 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 7 5.1E-02 0 0
CUI: C4706469
Disease: X-linked Charcot-Marie-Tooth disease type 5
X-linked Charcot-Marie-Tooth disease type 5 		1 0 1 1.3E-02 0 0
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia 		68 0 1 6.8E-03 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 1 7.4E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 7 2.9E-02 0 0
CUI: C0262478
Disease: Wrinkled face
Wrinkled face 		5 0 1 1.2E-02 0 0
CUI: C0043207
Disease: Wolfram Syndrome
Wolfram Syndrome 		28 0 1 9.4E-03 0 0
CUI: C4310804
Disease: WITTEVEEN-KOLK SYNDROME
WITTEVEEN-KOLK SYNDROME 		1 0 1 1.3E-02 0 0