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: C0267509
Disease: Chronic idiopathic constipation
Chronic idiopathic constipation 		5 0 5 0.45 0 0
CUI: C0687713
Disease: Gastrointestinal Pain
Gastrointestinal Pain 		3 0 3 0.27 0 0
CUI: C3160897
Disease: Opioid-Induced Constipation
Opioid-Induced Constipation 		8 0 3 0.19 0 0
CUI: C3472181
Disease: Severe dehydration
Severe dehydration 		3 0 2 0.17 0 0
CUI: C0401146
Disease: Constipation - functional
Constipation - functional 		15 0 3 0.13 0 0
CUI: C0232491
Disease: Chronic abdominal pain
Chronic abdominal pain 		9 0 2 0.11 0 0
CUI: C0277528
Disease: Traveler's diarrhea
Traveler's diarrhea 		21 0 3 0.10 0 0
CUI: C0033936
Disease: Psychoses, Alcoholic
Psychoses, Alcoholic 		1 0 1 9.1E-02 0 0
CUI: C2750893
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 11 		1 0 1 9.1E-02 0 0
CUI: C3810242
Disease: LEUKOENCEPHALOPATHY WITH ATAXIA
LEUKOENCEPHALOPATHY WITH ATAXIA 		1 0 1 9.1E-02 0 0
CUI: C4554120
Disease: Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Leukoencephalopathy with mild cerebellar ataxia and white matter edema 		1 0 1 9.1E-02 0 0
CUI: C0154934
Disease: Peripheral anterior synechiae
Peripheral anterior synechiae 		2 0 1 8.3E-02 0 0
CUI: C0232602
Disease: Retching
Retching 		2 0 1 8.3E-02 0 0
CUI: C3713420
Disease: Familial Hyperaldosteronism
Familial Hyperaldosteronism 		15 0 2 8.3E-02 0 0
CUI: C3850153
Disease: Ovarian Reserve
Ovarian Reserve 		2 0 1 8.3E-02 0 0
CUI: C4021591
Disease: Reduced number of intrahepatic bile ducts
Reduced number of intrahepatic bile ducts 		2 0 1 8.3E-02 0 0
CUI: C0344263
Disease: Posterior lenticonus
Posterior lenticonus 		3 0 1 7.7E-02 0 0
CUI: C0740432
Disease: Stomach fullness
Stomach fullness 		3 0 1 7.7E-02 0 0
CUI: C1847165
Disease: Generalized tonic-clonic seizures on awakening
Generalized tonic-clonic seizures on awakening 		3 0 1 7.7E-02 0 0
CUI: C1865869
Disease: CONE DYSTROPHY 3 (disorder)
CONE DYSTROPHY 3 (disorder) 		3 0 1 7.7E-02 0 0
CUI: C3553270
Disease: DIARRHEA 6
DIARRHEA 6 		3 0 1 7.7E-02 0 0
CUI: C4021086
Disease: Abnormal biliary tract morphology
Abnormal biliary tract morphology 		3 0 1 7.7E-02 0 0
CUI: C4023208
Disease: Glucocortocoid-insensitive primary hyperaldosteronism
Glucocortocoid-insensitive primary hyperaldosteronism 		3 0 1 7.7E-02 0 0
CUI: C0267663
Disease: Congenital secretory diarrhea, sodium type (disorder)
Congenital secretory diarrhea, sodium type (disorder) 		18 0 2 7.4E-02 0 0
CUI: C0267557
Disease: Secretory diarrhea
Secretory diarrhea 		19 0 2 7.1E-02 0 0