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: C3275899
Disease: Hyperechogenic kidneys
Hyperechogenic kidneys 		12 0 1 8.3E-02 0 0
CUI: C0549613
Disease: Biliary tract abnormality
Biliary tract abnormality 		14 0 1 7.1E-02 0 0
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 1 7.1E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst 		26 0 1 3.8E-02 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts 		46 0 1 2.2E-02 0 0
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst 		60 0 1 1.7E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		63 0 1 1.6E-02 0 0
CUI: C0085548
Disease: Autosomal Recessive Polycystic Kidney Disease
Autosomal Recessive Polycystic Kidney Disease 		69 0 1 1.4E-02 0 0
CUI: C1857453
Disease: Renal hypoplasia/aplasia
Renal hypoplasia/aplasia 		73 0 1 1.4E-02 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 8.5E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 6.1E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 5.3E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		223 0 1 4.5E-03 0 0
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases 		276 0 1 3.6E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		315 0 1 3.2E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		319 0 1 3.1E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 0 1 1.7E-03 0 0
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		615 0 1 1.6E-03 0 0
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		666 0 1 1.5E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 1 1.2E-03 0 0