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 8.1E-03 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 1 3.7E-03 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 5 1.4E-02 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome 		13 0 11 6.0E-02 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 14 6.9E-02 0 0
CUI: C4687396
Disease: Zellweger Spectrum Disorder
Zellweger Spectrum Disorder 		6 0 4 2.2E-02 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 12 6.3E-02 0 0
CUI: C0270969
Disease: Zebra body myopathy
Zebra body myopathy 		4 0 1 5.5E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 4 1.6E-02 0 0
CUI: C1866425
Disease: Yemenite deaf-blind hypopigmentation syndrome
Yemenite deaf-blind hypopigmentation syndrome 		1 0 1 5.6E-03 0 0
CUI: C0043395
Disease: Yellow Fever
Yellow Fever 		28 0 1 4.8E-03 0 0
CUI: C4505432
Disease: XMRV Infection
XMRV Infection 		6 0 1 5.4E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 2 8.5E-03 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 1 4.4E-03 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 1 4.0E-03 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 1 4.0E-03 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 1 4.6E-03 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 3 1.5E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 5.6E-03 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly 		14 0 5 2.6E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 4 1.7E-02 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 4 1.7E-02 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 3 1.3E-02 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 9 2.6E-02 0 0
CUI: C0241760
Disease: Wrist swelling
Wrist swelling 		2 0 1 5.5E-03 0 0