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: C1969875
Disease: Beta-cell dysfunction
Beta-cell dysfunction
6 0 5 0.45 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells
7 0 5 0.42 0 0
Neonatal insulin-dependent diabetes mellitus
10 0 5 0.33 0 0
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
3 0 3 0.30 0 0
Hyperinsulinemic hypoglycemia, familial, 1
3 0 3 0.30 0 0
Hyperinsulinemic hypoglycemia, familial, 2
3 0 3 0.30 0 0
Contractures of the joints of the lower limbs
12 0 5 0.29 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes
8 0 4 0.29 0 0
Developmental Delay, Epilepsy, and Neonatal Diabetes
4 0 3 0.27 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c
14 0 5 0.26 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 5 0.26 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 5 0.25 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas
20 0 5 0.20 0 0
Diabetes mellitus autosomal dominant type II (disorder)
8 0 3 0.20 0 0
DIABETES MELLITUS, PERMANENT NEONATAL
20 0 5 0.20 0 0
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
2 0 2 0.20 0 0
CUI: C4022484
Disease: Clinodactyly of the 4th finger
Clinodactyly of the 4th finger
2 0 2 0.20 0 0
CUI: C4303593
Disease: DEND syndrome
DEND syndrome
3 0 2 0.18 0 0
Transient neonatal diabetes mellitus
23 0 5 0.18 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome
10 0 3 0.18 0 0
Non-insulin-dependent diabetes mellitus with unspecified complications
4 0 2 0.17 0 0
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
4 0 2 0.17 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria
26 0 5 0.16 0 0
CUI: C0027773
Disease: Nesidioblastosis
Nesidioblastosis
12 0 3 0.16 0 0
Diabetes Mellitus, Transient Neonatal, 1
12 0 3 0.16 0 0