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: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
276 54 71 0.20 2 2.9E-02
Polycystic Kidney, Autosomal Dominant
280 0 59 0.16 0 0
CUI: C3887499
Disease: Renal cyst
Renal cyst
170 17 38 0.13 2 6.1E-02
CUI: C0022679
Disease: Cystic kidney
Cystic kidney
89 0 26 0.12 0 0
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
212 0 39 0.12 0 0
Autosomal Recessive Polycystic Kidney Disease
69 0 23 0.12 0 0
CUI: C0151718
Disease: Hypocholesterolemia
Hypocholesterolemia
113 0 27 0.11 0 0
CUI: C0149939
Disease: Obstructive nephropathy
Obstructive nephropathy
95 0 25 0.11 0 0
CUI: C1867441
Disease: Pterygium Of Conjunctiva And Cornea
Pterygium Of Conjunctiva And Cornea
169 0 32 0.11 0 0
CUI: C4520843
Disease: Pterygium of eye
Pterygium of eye
169 0 32 0.11 0 0
CUI: C0521607
Disease: Peritoneal Fibrosis
Peritoneal Fibrosis
104 0 25 0.11 0 0
CUI: C0008373
Disease: Cholesteatoma
Cholesteatoma
135 0 28 0.11 0 0
CUI: C0010709
Disease: Cyst
Cyst
221 0 35 0.10 0 0
CUI: C0265101
Disease: Carotid artery occlusion
Carotid artery occlusion
74 0 21 0.10 0 0
CUI: C0751674
Disease: Lymphangioleiomyomatosis
Lymphangioleiomyomatosis
96 0 23 0.10 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
270 0 39 0.10 0 0
CUI: C0853897
Disease: Diabetic Cardiomyopathies
Diabetic Cardiomyopathies
220 0 34 0.10 0 0
CUI: C0015923
Disease: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome
89 0 22 1.0E-01 0 0
TNF receptor-associated periodic fever syndrome (TRAPS)
90 0 22 1.0E-01 0 0
CUI: C0041341
Disease: Tuberous Sclerosis
Tuberous Sclerosis
289 0 40 1.0E-01 0 0
CUI: C1260954
Disease: Morphologically altered structure
Morphologically altered structure
46 0 18 9.9E-02 0 0
CUI: C0033999
Disease: Pterygium
Pterygium
216 0 33 9.8E-02 0 0
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
328 0 43 9.8E-02 0 0
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3
209 0 32 9.7E-02 0 0
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
130 0 25 9.7E-02 0 0