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: C0267557
Disease: Secretory diarrhea
Secretory diarrhea 		19 2 5 0.15 2 0.12
CUI: C2751260
Disease: Macrothrombocytopenia
Macrothrombocytopenia 		34 0 5 0.10 0 0
CUI: C0267662
Disease: Congenital chloride diarrhea
Congenital chloride diarrhea 		3 0 2 1.0E-01 0 0
CUI: C0037859
Disease: Spermatocele
Spermatocele 		5 0 2 9.1E-02 0 0
CUI: C0239182
Disease: Watery diarrhoea
Watery diarrhoea 		5 0 2 9.1E-02 0 0
CUI: C0268312
Disease: Progressive intrahepatic cholestasis (disorder)
Progressive intrahepatic cholestasis (disorder) 		31 0 4 8.7E-02 0 0
CUI: C0268181
Disease: Lactose Intolerance, Adult Type
Lactose Intolerance, Adult Type 		7 0 2 8.3E-02 0 0
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 2 8.3E-02 0 0
CUI: C0342488
Disease: Mineralocorticoid Excess Syndrome, Apparent
Mineralocorticoid Excess Syndrome, Apparent 		8 0 2 8.0E-02 0 0
CUI: C0085679
Disease: Hyperchloremia
Hyperchloremia 		12 2 2 6.9E-02 2 0.12
CUI: C0151746
Disease: Abnormal renal function
Abnormal renal function 		12 0 2 6.9E-02 0 0
CUI: C0033817
Disease: Pseudomonas Infections
Pseudomonas Infections 		16 0 2 6.1E-02 0 0
CUI: C0034089
Disease: Pulmonary Valve Stenosis
Pulmonary Valve Stenosis 		16 0 2 6.1E-02 0 0
CUI: C4551482
Disease: Adams-Oliver syndrome 1
Adams-Oliver syndrome 1 		17 0 2 5.9E-02 0 0
CUI: C0030389
Disease: Parainfluenza
Parainfluenza 		36 0 3 5.8E-02 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency 		18 0 2 5.7E-02 0 0
CUI: C0546884
Disease: Hypovolemia
Hypovolemia 		37 0 3 5.7E-02 0 0
CUI: C0267456
Disease: Villous atrophy of intestine
Villous atrophy of intestine 		19 0 2 5.6E-02 0 0
CUI: C0554101
Disease: Villous atrophy
Villous atrophy 		19 0 2 5.6E-02 0 0
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		38 0 3 5.6E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 5.3E-02 0 0
CUI: C0034066
Disease: Pulmonary embolism with pulmonary infarction
Pulmonary embolism with pulmonary infarction 		1 0 1 5.3E-02 0 0
CUI: C0155820
Disease: Acute bronchitis and bronchiolitis
Acute bronchitis and bronchiolitis 		1 0 1 5.3E-02 0 0
CUI: C0155833
Disease: Hyperplasia of adenoids
Hyperplasia of adenoids 		1 0 1 5.3E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 5.3E-02 0 0