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: C0235950
Disease: Zinc deficiency
Zinc deficiency 		90 0 3 1.7E-02 0 0
CUI: C0751594
Disease: Zellweger-Like Syndrome
Zellweger-Like Syndrome 		13 0 1 9.5E-03 0 0
CUI: C0043459
Disease: Zellweger Syndrome
Zellweger Syndrome 		36 0 2 1.6E-02 0 0
CUI: C4687396
Disease: Zellweger Spectrum Disorder
Zellweger Spectrum Disorder 		6 0 1 1.0E-02 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum 		21 0 2 1.8E-02 0 0
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		51 0 1 7.0E-03 0 0
CUI: C0014145
Disease: Yolk Sac Tumor
Yolk Sac Tumor 		68 0 1 6.3E-03 0 0
CUI: C0043395
Disease: Yellow Fever
Yellow Fever 		28 0 1 8.3E-03 0 0
CUI: C0432475
Disease: XX males
XX males 		32 0 1 8.1E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 4 2.8E-02 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 2 1.8E-02 0 0
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		8 0 2 2.0E-02 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 1 9.5E-03 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 55 2 1.4E-02 2 2.7E-02
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 2 1.2E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 2 1.3E-02 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 3 1.3E-02 0 0
CUI: C0043345
Disease: Xeroderma
Xeroderma 		7 0 1 1.0E-02 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 1 7.6E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 1 6.9E-03 0 0
CUI: C3275445
Disease: X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia 		11 0 1 9.7E-03 0 0
CUI: C0241932
Disease: X-linked hypogammaglobulinemia
X-linked hypogammaglobulinemia 		4 0 1 1.0E-02 0 0
CUI: C4304400
Disease: X-linked hereditary sensory and autonomic neuropathy with deafness
X-linked hereditary sensory and autonomic neuropathy with deafness 		1 0 1 1.1E-02 0 0
CUI: C4551551
Disease: X-linked hereditary motor and sensory neuropathy
X-linked hereditary motor and sensory neuropathy 		7 0 2 2.0E-02 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 2 1.3E-02 0 0