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 1 7.1E-03 0 0
CUI: C0043528
Disease: Zoonoses
Zoonoses 		19 0 1 1.1E-02 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 1 6.2E-03 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 1 3.8E-03 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome 		13 0 1 1.2E-02 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 3 2.9E-02 0 0
CUI: C4687396
Disease: Zellweger Spectrum Disorder
Zellweger Spectrum Disorder 		6 0 2 2.6E-02 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 1 1.1E-02 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 8.2E-03 0 0
CUI: C1863008
Disease: Yellow-brown discoloration of the teeth
Yellow-brown discoloration of the teeth 		7 0 1 1.3E-02 0 0
CUI: C4310620
Disease: Yao syndrome
Yao syndrome 		5 0 1 1.3E-02 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 1 7 5.8E-02 1 4.2E-02
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 1 7.1E-03 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 1 7.1E-03 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 2 1.8E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 1 1.1E-02 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum 		15 0 1 1.2E-02 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 1 1.0E-02 0 0
CUI: C0751605
Disease: X-Linked, Spastic Paraplegia, Hereditary
X-Linked, Spastic Paraplegia, Hereditary 		5 0 1 1.3E-02 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 1 1.0E-02 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 2 2.4E-02 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly 		14 0 1 1.2E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 122 3 2.5E-02 1 6.9E-03
CUI: C4551551
Disease: X-linked hereditary motor and sensory neuropathy
X-linked hereditary motor and sensory neuropathy 		7 0 1 1.3E-02 0 0
CUI: C0751337
Disease: X-Linked Emery-Dreifuss Muscular Dystrophy
X-Linked Emery-Dreifuss Muscular Dystrophy 		20 0 1 1.1E-02 0 0