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: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 6 1.9E-02 0 0
CUI: C1848411
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E 		9 0 1 3.5E-03 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 4 1.2E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 12 3.6E-02 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 12 3.0E-02 0 0
CUI: C0043345
Disease: Xeroderma
Xeroderma 		7 0 1 3.5E-03 0 0
CUI: C0272051
Disease: Xerocytosis
Xerocytosis 		20 0 3 1.0E-02 0 0
CUI: C0457190
Disease: Xanthomatous Meningioma
Xanthomatous Meningioma 		12 0 3 1.0E-02 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 7 2.2E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 4 1.4E-02 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum 		15 0 3 1.0E-02 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 1 3.2E-03 0 0
CUI: C1337035
Disease: Xanthogranulomatous cholecystitis
Xanthogranulomatous cholecystitis 		6 0 1 3.5E-03 0 0
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 2 6.5E-03 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 1 3.4E-03 0 0
CUI: C0549463
Disease: X-Linked Lymphoproliferative Disorder
X-Linked Lymphoproliferative Disorder 		49 0 1 3.0E-03 0 0
CUI: C2828000
Disease: X-Linked Inherited Disorder
X-Linked Inherited Disorder 		3 0 2 7.1E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 3 9.1E-03 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 1 3.3E-03 0 0
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita 		17 0 2 6.8E-03 0 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance 		65 0 2 5.8E-03 0 0
CUI: C1279481
Disease: X-Linked Combined Immunodeficiency Diseases
X-Linked Combined Immunodeficiency Diseases 		38 0 2 6.3E-03 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 1 3.2E-03 0 0
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia 		68 0 8 2.4E-02 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 4 1.2E-02 0 0