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: C0016807
Disease: Functional disorder of intestine
Functional disorder of intestine 		4 0 2 0.20 0 0
CUI: C0853892
Disease: Catabolic state
Catabolic state 		8 0 2 0.14 0 0
CUI: C4054325
Disease: Obesity Related Glomerulopathy
Obesity Related Glomerulopathy 		16 0 3 0.14 0 0
CUI: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 0.12 0 0
CUI: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		1 0 1 0.12 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis 		1 0 1 0.12 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder 		1 0 1 0.12 0 0
CUI: C0268457
Disease: Aminoacidemia
Aminoacidemia 		1 0 1 0.12 0 0
CUI: C0270217
Disease: Perinatal jaundice due to inspissated bile syndrome
Perinatal jaundice due to inspissated bile syndrome 		1 0 1 0.12 0 0
CUI: C0271712
Disease: Hypoglycemia of childhood
Hypoglycemia of childhood 		1 0 1 0.12 0 0
CUI: C0302874
Disease: Depressive personality disorder
Depressive personality disorder 		1 0 1 0.12 0 0
CUI: C0341274
Disease: Acute radiation enteritis
Acute radiation enteritis 		1 0 1 0.12 0 0
CUI: C0948393
Disease: Oedematous pancreatitis
Oedematous pancreatitis 		1 0 1 0.12 0 0
CUI: C1881406
Disease: Lipase Hypersecretion Syndrome
Lipase Hypersecretion Syndrome 		1 0 1 0.12 0 0
CUI: C1970270
Disease: Choreoathetosis And Congenital Hypothyroidism
Choreoathetosis And Congenital Hypothyroidism 		1 0 1 0.12 0 0
CUI: C2939096
Disease: Pulmonary sensitisation
Pulmonary sensitisation 		1 0 1 0.12 0 0
CUI: C3203523
Disease: Acute repetitive seizure
Acute repetitive seizure 		1 0 1 0.12 0 0
CUI: C3249879
Disease: Combat Fatigue
Combat Fatigue 		1 0 1 0.12 0 0
CUI: C3266628
Disease: Persistent asthma
Persistent asthma 		1 0 1 0.12 0 0
CUI: C4016279
Disease: LEPTIN DYSFUNCTION
LEPTIN DYSFUNCTION 		1 0 1 0.12 0 0
CUI: C4022657
Disease: Abnormal drinking behavior
Abnormal drinking behavior 		1 0 1 0.12 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome 		1 0 1 0.12 0 0
CUI: C4476847
Disease: Short bowel
Short bowel 		1 0 1 0.12 0 0
CUI: C4721429
Disease: THYROID CANCER, NONMEDULLARY, 1
THYROID CANCER, NONMEDULLARY, 1 		1 0 1 0.12 0 0
CUI: C0036992
Disease: Short Bowel Syndrome
Short Bowel Syndrome 		21 0 3 0.12 0 0