Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Diabetes mellitus autosomal dominant type II (disorder)
8 0 4 0.25 0 0
Maturity-Onset Diabetes of the Young, Type 1
4 0 3 0.23 0 0
CUI: C4330695
Disease: Mitochondrial Diabetes
Mitochondrial Diabetes
7 0 3 0.19 0 0
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode
8 0 3 0.18 0 0
CUI: C0239233
Disease: Early satiety
Early satiety
2 0 2 0.17 0 0
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism
2 0 2 0.17 0 0
DIABETES MELLITUS, INSULIN-DEPENDENT, 20 (disorder)
2 7 2 0.17 4 7.8E-02
CUI: C4274352
Disease: Chronic intestinal failure
Chronic intestinal failure
3 0 2 0.15 0 0
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
4 0 2 0.14 0 0
CUI: C0149670
Disease: Disorder of carbohydrate metabolism
Disorder of carbohydrate metabolism
5 0 2 0.13 0 0
CUI: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome
5 0 2 0.13 0 0
CUI: C3826457
Disease: Diabetes in children
Diabetes in children
22 0 4 0.13 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c
14 0 3 0.13 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 3 0.13 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 3 0.12 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia
15 0 3 0.12 0 0
Papillary cystadenoma of the epididymis
6 0 2 0.12 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes
8 0 2 0.11 0 0
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
30 0 4 0.11 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas
20 0 3 0.10 0 0
DIABETES MELLITUS, PERMANENT NEONATAL
20 0 3 0.10 0 0
CUI: C1257958
Disease: Glucose Metabolism Disorders
Glucose Metabolism Disorders
32 0 4 1.0E-01 0 0
CUI: C0017980
Disease: Glycosuria, Renal
Glycosuria, Renal
11 17 2 9.5E-02 1 1.6E-02
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome
11 0 2 9.5E-02 0 0
Transient neonatal diabetes mellitus
23 0 3 9.4E-02 0 0