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: C1970416
Disease: XFE Progeroid Syndrome
XFE Progeroid Syndrome 		3 0 1 0.11 0 0
CUI: C1968561
Disease: Xeroderma Pigmentosum, Type G-Cockayne Syndrome
Xeroderma Pigmentosum, Type G-Cockayne Syndrome 		2 0 1 0.12 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 4 0.17 0 0
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		8 31 1 7.1E-02 1 1.1E-02
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 2 0.11 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 4 7.8E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 111 5 6.9E-02 4 2.4E-02
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 2 2.7E-02 0 0
CUI: C1970808
Disease: Xeroderma Pigmentosum B-Cockayne Syndrome
Xeroderma Pigmentosum B-Cockayne Syndrome 		1 0 1 0.14 0 0
CUI: C4304411
Disease: Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum and Cockayne syndrome complex 		10 0 3 0.21 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 35 7 5.1E-02 4 4.5E-02
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		96 0 1 9.8E-03 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		130 0 1 7.4E-03 0 0
CUI: C0751396
Disease: Well Differentiated Oligodendroglioma
Well Differentiated Oligodendroglioma 		270 0 1 3.6E-03 0 0
CUI: C0042963
Disease: Vomiting
Vomiting 		303 0 1 3.2E-03 0 0
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		302 0 1 3.2E-03 0 0
CUI: C0042900
Disease: Vitiligo
Vitiligo 		395 0 1 2.5E-03 0 0
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		422 0 4 9.4E-03 0 0
CUI: C0266999
Disease: Vesicular Stomatitis
Vesicular Stomatitis 		112 0 2 1.7E-02 0 0
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		69 0 4 5.6E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		426 0 2 4.6E-03 0 0
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		378 0 1 2.6E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 2 6.2E-03 0 0
CUI: C3551173
Disease: UV-SENSITIVE SYNDROME 1
UV-SENSITIVE SYNDROME 1 		1 5 1 0.14 4 6.8E-02
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		15 0 6 0.38 0 0