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 0.10 0 0
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		46 0 8 0.10 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance 		15 0 5 0.10 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 10 1.0E-01 0 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney 		27 0 6 1.0E-01 0 0
CUI: C0151747
Disease: Renal tubular disorder
Renal tubular disorder 		64 0 9 9.6E-02 0 0
CUI: C0220722
Disease: Cerebrooculofacioskeletal Syndrome 1
Cerebrooculofacioskeletal Syndrome 1 		7 0 4 9.5E-02 0 0
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		30 0 6 9.5E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 10 9.3E-02 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes 		8 0 4 9.3E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma 		34 0 6 9.0E-02 0 0
CUI: C1859455
Disease: Small anterior fontanelle
Small anterior fontanelle 		11 4 4 8.7E-02 1 0.20
CUI: C0027773
Disease: Nesidioblastosis
Nesidioblastosis 		12 0 4 8.5E-02 0 0
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia 		52 0 7 8.3E-02 0 0
CUI: C0497406
Disease: Overweight
Overweight 		27 0 5 8.2E-02 0 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive 		14 0 4 8.2E-02 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		122 0 12 8.1E-02 0 0
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		30 0 5 7.8E-02 0 0
CUI: C1833102
Disease: DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES 		3 0 3 7.7E-02 0 0
CUI: C1859312
Disease: CAMFAK syndrome
CAMFAK syndrome 		3 0 3 7.7E-02 0 0
CUI: C2931277
Disease: Pena Shokeir syndrome Type 2
Pena Shokeir syndrome Type 2 		3 0 3 7.7E-02 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 0 3 7.7E-02 0 0
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		3 0 3 7.7E-02 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 3 7.5E-02 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 10 7.5E-02 0 0