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: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 5 3 0.75 3 0.27
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		2 15 2 0.67 1 4.3E-02
CUI: C4022484
Disease: Clinodactyly of the 4th finger
Clinodactyly of the 4th finger 		2 0 2 0.67 0 0
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction 		6 0 3 0.50 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 0 2 0.50 0 0
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		3 0 2 0.50 0 0
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		3 8 2 0.50 4 0.31
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells 		7 0 3 0.43 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		8 0 3 0.38 0 0
CUI: C0022492
Disease: Kandinsky Syndrome
Kandinsky Syndrome 		1 0 1 0.33 0 0
CUI: C0023213
Disease: Ventricular Outflow Obstruction, Left
Ventricular Outflow Obstruction, Left 		1 0 1 0.33 0 0
CUI: C0028313
Disease: Organic Brain Syndrome, Nonpsychotic
Organic Brain Syndrome, Nonpsychotic 		1 0 1 0.33 0 0
CUI: C0029230
Disease: Organic Mental Disorders, Psychotic
Organic Mental Disorders, Psychotic 		1 0 1 0.33 0 0
CUI: C0033943
Disease: Psychoses, Traumatic
Psychoses, Traumatic 		1 0 1 0.33 0 0
CUI: C0035619
Disease: Ventricular Outflow Obstruction, Right
Ventricular Outflow Obstruction, Right 		1 0 1 0.33 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction 		1 0 1 0.33 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 0.33 0 0
CUI: C0270221
Disease: Syndrome of infant of diabetic mother
Syndrome of infant of diabetic mother 		1 0 1 0.33 0 0
CUI: C0270730
Disease: MPTP Poisoning
MPTP Poisoning 		1 0 1 0.33 0 0
CUI: C0271703
Disease: Factitious hypoglycemia
Factitious hypoglycemia 		1 0 1 0.33 0 0
CUI: C0271714
Disease: Hypoglycemia, leucine-induced
Hypoglycemia, leucine-induced 		1 0 1 0.33 0 0
CUI: C0751864
Disease: MPTP-Induced Degeneration of the Striatum
MPTP-Induced Degeneration of the Striatum 		1 0 1 0.33 0 0
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 0 1 0.33 0 0
CUI: C4225365
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13 		1 0 1 0.33 0 0
CUI: C4274080
Disease: Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency 		1 0 1 0.33 0 0