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: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		1 2 1 1.9E-02 1 9.2E-03
CUI: C3549845
Disease: CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1 		1 0 1 1.9E-02 0 0
CUI: C4025019
Disease: Intrahepatic cholestasis with episodic jaundice
Intrahepatic cholestasis with episodic jaundice 		1 0 1 1.9E-02 0 0
CUI: C4025808
Disease: Facial flushing after alcohol intake
Facial flushing after alcohol intake 		1 0 1 1.9E-02 0 0
CUI: C4225229
Disease: CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES
CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES 		1 0 1 1.9E-02 0 0
CUI: C4303475
Disease: Hyperinsulinism due to HNF1A deficiency
Hyperinsulinism due to HNF1A deficiency 		1 0 1 1.9E-02 0 0
CUI: C4693925
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65 		1 0 1 1.9E-02 0 0
CUI: C4747984
Disease: PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA
PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA 		1 0 1 1.9E-02 0 0
CUI: C4748041
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA
INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA 		1 0 1 1.9E-02 0 0
CUI: C4748341
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67 		1 0 1 1.9E-02 0 0
CUI: C0008352
Disease: Cholemia
Cholemia 		2 0 1 1.8E-02 0 0
CUI: C0206044
Disease: Infections, Calicivirus
Infections, Calicivirus 		2 0 1 1.8E-02 0 0
CUI: C0403502
Disease: Low renal threshold for glucose
Low renal threshold for glucose 		2 0 1 1.8E-02 0 0
CUI: C0585229
Disease: Multiple lacunar infarcts
Multiple lacunar infarcts 		2 0 1 1.8E-02 0 0
CUI: C1842462
Disease: CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL 		2 0 1 1.8E-02 0 0
CUI: C1858114
Disease: HUNTINGTON DISEASE-LIKE 3 (disorder)
HUNTINGTON DISEASE-LIKE 3 (disorder) 		2 0 1 1.8E-02 0 0
CUI: C2675866
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)
DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder) 		2 0 2 3.7E-02 0 0
CUI: C3554241
Disease: CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3
CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3 		2 0 1 1.8E-02 0 0
CUI: C3826291
Disease: Gastroenteritis in children
Gastroenteritis in children 		2 0 1 1.8E-02 0 0
CUI: C4021882
Disease: Increased serum bile acid concentration during pregnancy
Increased serum bile acid concentration during pregnancy 		2 0 1 1.8E-02 0 0
CUI: C4022392
Disease: Early onset of sexual maturation
Early onset of sexual maturation 		2 0 1 1.8E-02 0 0
CUI: C4304531
Disease: 2q32q33 microdeletion syndrome
2q32q33 microdeletion syndrome 		2 0 1 1.8E-02 0 0
CUI: C4552322
Disease: Obesity cardiomyopathy
Obesity cardiomyopathy 		2 0 1 1.8E-02 0 0
CUI: C0031051
Disease: Pericementitis
Pericementitis 		3 0 1 1.8E-02 0 0
CUI: C0158698
Disease: Congenital malformation of the urinary system
Congenital malformation of the urinary system 		3 0 1 1.8E-02 0 0