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: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens 		1 0 1 5.0E-02 0 0
CUI: C1306162
Disease: Kidney replacement disorder
Kidney replacement disorder 		1 0 1 5.0E-02 0 0
CUI: C1567427
Disease: Bilateral Multicystic Dysplastic Kidneys
Bilateral Multicystic Dysplastic Kidneys 		1 0 1 5.0E-02 0 0
CUI: C1833999
Disease: Retinal pigmentary degeneration
Retinal pigmentary degeneration 		1 0 1 5.0E-02 0 0
CUI: C1835934
Disease: Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria 		1 0 1 5.0E-02 0 0
CUI: C1836946
Disease: Peripheral Cone Dystrophy
Peripheral Cone Dystrophy 		1 0 1 5.0E-02 0 0
CUI: C1837464
Disease: Small eyes
Small eyes 		1 0 1 5.0E-02 0 0
CUI: C1844776
Disease: CONE-ROD DYSTROPHY, X-LINKED, 1
CONE-ROD DYSTROPHY, X-LINKED, 1 		1 0 1 5.0E-02 0 0
CUI: C1847013
Disease: NEPHRONOPHTHISIS 4
NEPHRONOPHTHISIS 4 		1 0 1 5.0E-02 0 0
CUI: C1849198
Disease: Opacification of the corneal epithelium
Opacification of the corneal epithelium 		1 0 1 5.0E-02 0 0
CUI: C1857780
Disease: JOUBERT SYNDROME 5
JOUBERT SYNDROME 5 		1 0 1 5.0E-02 0 0
CUI: C1857821
Disease: LEBER CONGENITAL AMAUROSIS 10 (disorder)
LEBER CONGENITAL AMAUROSIS 10 (disorder) 		1 0 1 5.0E-02 0 0
CUI: C1865880
Disease: Hyperkalemic metabolic acidosis
Hyperkalemic metabolic acidosis 		1 0 1 5.0E-02 0 0
CUI: C1969052
Disease: MECKEL SYNDROME, TYPE 5
MECKEL SYNDROME, TYPE 5 		1 0 1 5.0E-02 0 0
CUI: C1969053
Disease: JOUBERT SYNDROME 7
JOUBERT SYNDROME 7 		1 0 1 5.0E-02 0 0
CUI: C1970161
Disease: MECKEL SYNDROME, TYPE 4
MECKEL SYNDROME, TYPE 4 		1 0 1 5.0E-02 0 0
CUI: C2749137
Disease: Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness 		1 0 1 5.0E-02 0 0
CUI: C2750475
Disease: Focal Segmental Glomerulosclerosis 5
Focal Segmental Glomerulosclerosis 5 		1 0 1 5.0E-02 0 0
CUI: C2959367
Disease: Nephronophthisis type 4
Nephronophthisis type 4 		1 0 1 5.0E-02 0 0
CUI: C3151784
Disease: MACULAR DEGENERATION, X-LINKED ATROPHIC
MACULAR DEGENERATION, X-LINKED ATROPHIC 		1 0 1 5.0E-02 0 0
CUI: C3280598
Disease: SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY
SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY 		1 0 1 5.0E-02 0 0
CUI: C3280612
Disease: NEPHRONOPHTHISIS 13
NEPHRONOPHTHISIS 13 		1 0 1 5.0E-02 0 0
CUI: C3280845
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E 		1 0 1 5.0E-02 0 0
CUI: C3541853
Disease: NEPHRONOPHTHISIS 15
NEPHRONOPHTHISIS 15 		1 0 1 5.0E-02 0 0
CUI: C3889474
Disease: BARDET-BIEDL SYNDROME 16
BARDET-BIEDL SYNDROME 16 		1 0 1 5.0E-02 0 0