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: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		30 0 4 0.11 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		42 0 5 0.11 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 2 0.11 0 0
CUI: C0022492
Disease: Kandinsky Syndrome
Kandinsky Syndrome 		1 0 1 1.0E-01 0 0
CUI: C0023213
Disease: Ventricular Outflow Obstruction, Left
Ventricular Outflow Obstruction, Left 		1 0 1 1.0E-01 0 0
CUI: C0028313
Disease: Organic Brain Syndrome, Nonpsychotic
Organic Brain Syndrome, Nonpsychotic 		1 0 1 1.0E-01 0 0
CUI: C0029230
Disease: Organic Mental Disorders, Psychotic
Organic Mental Disorders, Psychotic 		1 0 1 1.0E-01 0 0
CUI: C0033943
Disease: Psychoses, Traumatic
Psychoses, Traumatic 		1 0 1 1.0E-01 0 0
CUI: C0035619
Disease: Ventricular Outflow Obstruction, Right
Ventricular Outflow Obstruction, Right 		1 0 1 1.0E-01 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction 		1 0 1 1.0E-01 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 1.0E-01 0 0
CUI: C0270221
Disease: Syndrome of infant of diabetic mother
Syndrome of infant of diabetic mother 		1 0 1 1.0E-01 0 0
CUI: C0270730
Disease: MPTP Poisoning
MPTP Poisoning 		1 0 1 1.0E-01 0 0
CUI: C0271703
Disease: Factitious hypoglycemia
Factitious hypoglycemia 		1 0 1 1.0E-01 0 0
CUI: C0271714
Disease: Hypoglycemia, leucine-induced
Hypoglycemia, leucine-induced 		1 0 1 1.0E-01 0 0
CUI: C0597167
Disease: Islets of Langerhans hyperplasia
Islets of Langerhans hyperplasia 		12 0 2 1.0E-01 0 0
CUI: C0751864
Disease: MPTP-Induced Degeneration of the Striatum
MPTP-Induced Degeneration of the Striatum 		1 0 1 1.0E-01 0 0
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C2677132
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C4021554
Disease: Irregular tarsal ossification
Irregular tarsal ossification 		1 0 1 1.0E-01 0 0
CUI: C4023991
Disease: Ivory epiphyses of the toes
Ivory epiphyses of the toes 		1 0 1 1.0E-01 0 0
CUI: C4225195
Disease: MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2 		1 0 1 1.0E-01 0 0
CUI: C4225365
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13 		1 0 1 1.0E-01 0 0
CUI: C4274080
Disease: Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency 		1 0 1 1.0E-01 0 0
CUI: C4274081
Disease: Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency 		1 0 1 1.0E-01 0 0