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: C4303082
Disease: Hyperinsulinism due to uncoupling protein 2 deficiency
Hyperinsulinism due to uncoupling protein 2 deficiency 		1 0 1 1.00 0 0
CUI: C0678306
Disease: alcohol sensitivity
alcohol sensitivity 		3 0 1 0.33 0 0
CUI: C0392622
Disease: Toxic effect of carbon tetrachloride
Toxic effect of carbon tetrachloride 		6 0 1 0.17 0 0
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
Type 2 diabetes mellitus in obese 		7 0 1 0.14 0 0
CUI: C0451819
Disease: Simple obesity
Simple obesity 		9 0 1 0.11 0 0
CUI: C0887850
Disease: Polycystic Kidney, Type 1 Autosomal Dominant Disease
Polycystic Kidney, Type 1 Autosomal Dominant Disease 		10 0 1 1.0E-01 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 1 9.1E-02 0 0
CUI: C0597167
Disease: Islets of Langerhans hyperplasia
Islets of Langerhans hyperplasia 		12 0 1 8.3E-02 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia 		15 0 1 6.7E-02 0 0
CUI: C0393756
Disease: Hangover from alcohol
Hangover from alcohol 		16 0 1 6.2E-02 0 0
CUI: C0597048
Disease: Neurogenic hypertension
Neurogenic hypertension 		18 0 1 5.6E-02 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 1 3.2E-02 0 0
CUI: C1960636
Disease: Dysglycemia
Dysglycemia 		31 0 1 3.2E-02 0 0
CUI: C1257958
Disease: Glucose Metabolism Disorders
Glucose Metabolism Disorders 		32 0 1 3.1E-02 0 0
CUI: C1854838
Disease: Progressive neurologic deterioration
Progressive neurologic deterioration 		33 0 1 3.0E-02 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		37 0 1 2.7E-02 0 0
CUI: C1848395
Disease: Large for gestational age
Large for gestational age 		43 0 1 2.3E-02 0 0
CUI: C0262405
Disease: Cerebral dysfunction
Cerebral dysfunction 		45 0 1 2.2E-02 0 0
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia 		52 0 1 1.9E-02 0 0
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		55 0 1 1.8E-02 0 0
CUI: C0034372
Disease: Quadriplegia
Quadriplegia 		57 0 1 1.8E-02 0 0
CUI: C0085602
Disease: Polydipsia
Polydipsia 		61 0 1 1.6E-02 0 0
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism 		62 0 1 1.6E-02 0 0
CUI: C2750440
Disease: FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 		63 0 1 1.6E-02 0 0
CUI: C2750441
Disease: LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1
LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1 		63 0 1 1.6E-02 0 0