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: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial
1 4 1 0.50 4 0.57
Hyperinsulinism due to HNF1A deficiency
1 0 1 0.50 0 0
CUI: C0403502
Disease: Low renal threshold for glucose
Low renal threshold for glucose
2 0 1 0.33 0 0
Congenital malformation of the urinary system
3 0 1 0.25 0 0
Maturity-Onset Diabetes of the Young, Type 1
4 0 1 0.20 0 0
Decreased level of 1,5 anhydroglucitol in serum
4 0 1 0.20 0 0
Gamma glutamyl transferase measurement
5 0 1 0.17 0 0
CUI: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome
5 0 1 0.17 0 0
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
12 48 2 0.17 4 7.8E-02
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal
6 0 1 0.14 0 0
CUI: C0201952
Disease: Chloride measurement
Chloride measurement
16 0 2 0.12 0 0
CUI: C4330695
Disease: Mitochondrial Diabetes
Mitochondrial Diabetes
7 0 1 0.12 0 0
CUI: C4525496
Disease: Hamster Insulinoma
Hamster Insulinoma
7 0 1 0.12 0 0
Diabetes mellitus autosomal dominant type II (disorder)
8 0 1 0.11 0 0
CUI: C3828492
Disease: Pre-Gestational Diabetes
Pre-Gestational Diabetes
8 0 1 0.11 0 0
CUI: C4321446
Disease: K ATP Permanent Neonatal Diabetes
K ATP Permanent Neonatal Diabetes
8 0 1 0.11 0 0
CUI: C0017980
Disease: Glycosuria, Renal
Glycosuria, Renal
11 0 1 8.3E-02 0 0
CUI: C3658248
Disease: Hypertriglyceridemic Waist
Hypertriglyceridemic Waist
11 0 1 8.3E-02 0 0
CUI: C0597167
Disease: Islets of Langerhans hyperplasia
Islets of Langerhans hyperplasia
12 0 1 7.7E-02 0 0
CUI: C0496870
Disease: Benign neoplasm of liver
Benign neoplasm of liver
13 0 1 7.1E-02 0 0
CUI: C4073162
Disease: Elevated hemoglobin A1c
Elevated hemoglobin A1c
14 0 1 6.7E-02 0 0
CUI: C4280765
Disease: Abnormal C-peptide level
Abnormal C-peptide level
14 0 1 6.7E-02 0 0
CUI: C0862878
Disease: Dedifferentiated chondrosarcoma
Dedifferentiated chondrosarcoma
15 0 1 6.2E-02 0 0
CUI: C1847425
Disease: Abnormal oral glucose tolerance
Abnormal oral glucose tolerance
15 0 1 6.2E-02 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia
15 0 1 6.2E-02 0 0