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: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level 		14 0 5 0.24 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia 		15 0 5 0.23 0 0
CUI: C0796113
Disease: Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor 		7 0 3 0.19 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c 		14 0 4 0.18 0 0
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		8 0 3 0.18 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		8 0 3 0.18 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance 		15 0 4 0.17 0 0
CUI: C0271689
Disease: Insulin Receptor, Defect in
Insulin Receptor, Defect in 		2 0 2 0.17 0 0
CUI: C1839277
Disease: Submucous cleft lip
Submucous cleft lip 		2 0 2 0.17 0 0
CUI: C1839279
Disease: Six lumbar vertebrae
Six lumbar vertebrae 		2 0 2 0.17 0 0
CUI: C1839285
Disease: Two carpal ossification centers present at birth
Two carpal ossification centers present at birth 		2 0 2 0.17 0 0
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		2 0 2 0.17 0 0
CUI: C4022484
Disease: Clinodactyly of the 4th finger
Clinodactyly of the 4th finger 		2 0 2 0.17 0 0
CUI: C0158698
Disease: Congenital malformation of the urinary system
Congenital malformation of the urinary system 		3 0 2 0.15 0 0
CUI: C1833102
Disease: DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES 		3 0 2 0.15 0 0
CUI: C1839269
Disease: Duplication of renal pelvis
Duplication of renal pelvis 		3 0 2 0.15 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 0 2 0.15 0 0
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		3 0 2 0.15 0 0
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		3 0 2 0.15 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 3 0.15 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas 		20 0 4 0.14 0 0
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		20 0 4 0.14 0 0
CUI: C1839276
Disease: Broad secondary alveolar ridge
Broad secondary alveolar ridge 		4 0 2 0.14 0 0
CUI: C1852093
Disease: Maturity-Onset Diabetes of the Young, Type 1
Maturity-Onset Diabetes of the Young, Type 1 		4 0 2 0.14 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 2 0.14 0 0