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 8.3E-03 0 0
CUI: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 2 1.4E-02 0 0
CUI: C0276289
Disease: Zika Virus Infection
Zika Virus Infection 		192 0 3 1.2E-02 0 0
CUI: C0085232
Disease: Zenker Diverticulum
Zenker Diverticulum 		2 0 1 1.9E-02 0 0
CUI: C0270969
Disease: Zebra body myopathy
Zebra body myopathy 		4 0 1 1.8E-02 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 9.8E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 2 1.7E-02 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 1 1.0E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 1 8.3E-03 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 2 1.1E-02 0 0
CUI: C0457190
Disease: Xanthomatous Meningioma
Xanthomatous Meningioma 		12 0 1 1.6E-02 0 0
CUI: C1337035
Disease: Xanthogranulomatous cholecystitis
Xanthogranulomatous cholecystitis 		6 0 1 1.8E-02 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 0 1 1.5E-02 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 1 1.3E-02 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 2 3.1E-02 0 0
CUI: C0549463
Disease: X-Linked Lymphoproliferative Disorder
X-Linked Lymphoproliferative Disorder 		49 0 1 1.0E-02 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 9.6E-03 0 0
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita 		17 0 1 1.5E-02 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 1 8.6E-03 0 0
CUI: C0472813
Disease: X-linked agammaglobulinemia with growth hormone deficiency
X-linked agammaglobulinemia with growth hormone deficiency 		13 0 1 1.6E-02 0 0
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia 		68 0 1 8.4E-03 0 0
CUI: C4316810
Disease: Writer's Cramp
Writer's Cramp 		26 0 1 1.3E-02 0 0
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		48 0 1 1.0E-02 0 0
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		126 0 2 1.1E-02 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		95 0 2 1.4E-02 0 0