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: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 147 3 1.00 12 6.5E-02
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		2 15 2 0.67 11 0.20
CUI: C4022484
Disease: Clinodactyly of the 4th finger
Clinodactyly of the 4th finger 		2 0 2 0.67 0 0
CUI: C1833102
Disease: DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES 		3 0 2 0.50 0 0
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction 		6 0 3 0.50 0 0
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		3 0 2 0.50 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells 		7 0 3 0.43 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 2 0.40 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		8 0 3 0.38 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		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 6 1 0.33 2 3.7E-02
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 10 1 0.33 2 3.4E-02
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
Hyperinsulinemic hypoglycemia, familial, 3 		1 0 1 0.33 0 0
CUI: C2609269
Disease: Fasting hyperglycaemia
Fasting hyperglycaemia 		1 0 1 0.33 0 0
CUI: C4016117
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET 		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 5 1 0.33 1 1.9E-02
CUI: C4274080
Disease: Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency 		1 0 1 0.33 0 0
CUI: C4274081
Disease: Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency 		1 0 1 0.33 0 0
CUI: C1969879
Disease: Limb joint contracture
Limb joint contracture 		10 0 3 0.30 0 0
CUI: C3278636
Disease: Neonatal insulin-dependent diabetes mellitus
Neonatal insulin-dependent diabetes mellitus 		10 0 3 0.30 0 0
CUI: C4025043
Disease: Abnormality of the pancreatic islet cells
Abnormality of the pancreatic islet cells 		6 0 2 0.29 0 0
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism 		2 0 1 0.25 0 0
CUI: C1859523
Disease: Contractures of the joints of the lower limbs
Contractures of the joints of the lower limbs 		12 0 3 0.25 0 0
CUI: C2931207
Disease: Usher syndrome, type 1C
Usher syndrome, type 1C 		2 0 1 0.25 0 0