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: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 1.00 0 0
CUI: C0271703
Disease: Factitious hypoglycemia
Factitious hypoglycemia 		1 0 1 1.00 0 0
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 10 1 1.00 5 0.45
CUI: C4274080
Disease: Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency 		1 0 1 1.00 0 0
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		2 0 1 0.50 0 0
CUI: C2931207
Disease: Usher syndrome, type 1C
Usher syndrome, type 1C 		2 0 1 0.50 0 0
CUI: C4022484
Disease: Clinodactyly of the 4th finger
Clinodactyly of the 4th finger 		2 0 1 0.50 0 0
CUI: C1833102
Disease: DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES 		3 0 1 0.33 0 0
CUI: C1847555
Disease: Hyperinsulinemic hypoglycemia, familial, 6
Hyperinsulinemic hypoglycemia, familial, 6 		3 0 1 0.33 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 147 1 0.33 6 4.1E-02
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		3 50 1 0.33 2 3.7E-02
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		3 0 1 0.33 0 0
CUI: C1740821
Disease: Slowly progressive insulin dependent diabetes
Slowly progressive insulin dependent diabetes 		4 0 1 0.25 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 1 0.25 0 0
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction 		6 0 1 0.17 0 0
CUI: C3896643
Disease: New Onset Diabetes After Transplant
New Onset Diabetes After Transplant 		6 0 1 0.17 0 0
CUI: C4025043
Disease: Abnormality of the pancreatic islet cells
Abnormality of the pancreatic islet cells 		6 0 1 0.17 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells 		7 0 1 0.14 0 0
CUI: C4024168
Disease: Thickened ears
Thickened ears 		7 0 1 0.14 0 0
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		8 0 1 0.12 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		8 0 1 0.12 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		10 0 1 1.0E-01 0 0
CUI: C1969879
Disease: Limb joint contracture
Limb joint contracture 		10 0 1 1.0E-01 0 0
CUI: C3278636
Disease: Neonatal insulin-dependent diabetes mellitus
Neonatal insulin-dependent diabetes mellitus 		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