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: C0271271
Disease: Xerotic keratitis
Xerotic keratitis 		1 0 1 1.6E-03 0 0
CUI: C0043352
Disease: Xerostomia
Xerostomia 		56 0 11 1.7E-02 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 8 1.2E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 9 1.3E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 11 1.6E-02 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 18 2.5E-02 0 0
CUI: C0272051
Disease: Xerocytosis
Xerocytosis 		20 0 4 6.4E-03 0 0
CUI: C0457190
Disease: Xanthomatous Meningioma
Xanthomatous Meningioma 		12 0 4 6.4E-03 0 0
CUI: C0238052
Disease: Xanthomatosis, Cerebrotendinous
Xanthomatosis, Cerebrotendinous 		40 0 12 1.9E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 8 1.3E-02 0 0
CUI: C0221253
Disease: Xanthoma tendinosum
Xanthoma tendinosum 		15 0 6 9.6E-03 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma 		29 0 8 1.3E-02 0 0
CUI: C1337035
Disease: Xanthogranulomatous cholecystitis
Xanthogranulomatous cholecystitis 		6 0 2 3.2E-03 0 0
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 23 1 1.6E-03 1 3.3E-03
CUI: C0339528
Disease: X-linked retinitis pigmentosa
X-linked retinitis pigmentosa 		29 0 2 3.1E-03 0 0
CUI: C0271836
Disease: X-linked reduction of thyroxine-binding globulin
X-linked reduction of thyroxine-binding globulin 		1 0 1 1.6E-03 0 0
CUI: C1839615
Disease: X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy 		14 0 1 1.6E-03 0 0
CUI: C0549463
Disease: X-Linked Lymphoproliferative Disorder
X-Linked Lymphoproliferative Disorder 		49 0 12 1.8E-02 0 0
CUI: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly 		14 0 3 4.8E-03 0 0
CUI: C2828000
Disease: X-Linked Inherited Disorder
X-Linked Inherited Disorder 		3 0 1 1.6E-03 0 0
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		53 0 2 3.0E-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 1.6E-03 0 0
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 0 7 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 3.2E-03 0 0
CUI: C0751337
Disease: X-Linked Emery-Dreifuss Muscular Dystrophy
X-Linked Emery-Dreifuss Muscular Dystrophy 		20 0 2 3.2E-03 0 0