Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Contractures of the joints of the lower limbs
12 0 9 0.31 0 0
Neonatal insulin-dependent diabetes mellitus
10 0 8 0.29 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells
7 0 6 0.22 0 0
CUI: C0009421
Disease: Comatose
Comatose
78 0 17 0.20 0 0
Transient neonatal diabetes mellitus
23 0 8 0.20 0 0
Diabetes Mellitus, Transient Neonatal, 1
12 0 6 0.19 0 0
CUI: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction
6 0 5 0.19 0 0
Abnormality of the pancreatic islet cells
6 0 5 0.19 0 0
CUI: C0546884
Disease: Hypovolemia
Hypovolemia
37 0 9 0.17 0 0
CUI: C1969879
Disease: Limb joint contracture
Limb joint contracture
10 0 5 0.16 0 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge
39 0 9 0.16 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas
20 0 6 0.15 0 0
DIABETES MELLITUS, PERMANENT NEONATAL
20 0 6 0.15 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria
53 0 10 0.14 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c
14 0 5 0.14 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 5 0.14 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 5 0.14 0 0
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis
50 0 9 0.13 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
42 0 8 0.13 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes
8 0 4 0.13 0 0
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
30 0 6 0.12 0 0
CUI: C0022638
Disease: Ketosis
Ketosis
119 0 15 0.12 0 0
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
3 0 3 0.12 0 0
Hyperinsulinemic hypoglycemia, familial, 1
3 0 3 0.12 0 0
Hyperinsulinemic hypoglycemia, familial, 2
3 0 3 0.12 0 0