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, Insulin-Resistant, with Acanthosis Nigricans
1 0 1 0.50 0 0
Hyperinsulinemic Hypoglycemia, Familial, 5
1 0 1 0.50 0 0
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
1 0 1 0.50 0 0
Hyperinsulinism due to HNF4A deficiency
1 0 1 0.50 0 0
CUI: C0015938
Disease: Fetal Macrosomia
Fetal Macrosomia
2 0 1 0.33 0 0
CUI: C0263536
Disease: Hypertrophy of nail
Hypertrophy of nail
2 0 1 0.33 0 0
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism
2 0 1 0.33 0 0
CUI: C0333244
Disease: Transient edema
Transient edema
2 0 1 0.33 0 0
CUI: C0342337
Disease: Insulin resistance - type B
Insulin resistance - type B
2 0 1 0.33 0 0
CUI: C1855513
Disease: Prominent nipples
Prominent nipples
2 0 1 0.33 0 0
Idiopathic non-cirrhotic portal hypertension
2 0 1 0.33 0 0
CUI: C0342311
Disease: Neuroglycopenia
Neuroglycopenia
3 0 1 0.25 0 0
CUI: C0343047
Disease: Complement component 5 deficiency
Complement component 5 deficiency
3 0 1 0.25 0 0
CUI: C1854704
Disease: Metabolic Ketosis
Metabolic Ketosis
3 0 1 0.25 0 0
Abnormality of exocrine pancreas physiology
3 0 1 0.25 0 0
CUI: C4024615
Disease: Adipose tissue loss
Adipose tissue loss
3 0 1 0.25 0 0
CUI: C0029002
Disease: Onchocerciasis, Ocular
Onchocerciasis, Ocular
4 0 1 0.20 0 0
CUI: C0235430
Disease: Ketonemia
Ketonemia
4 0 1 0.20 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome
4 0 1 0.20 0 0
Maturity-Onset Diabetes of the Young, Type 1
4 0 1 0.20 0 0
CUI: C1854013
Disease: Anisomastia
Anisomastia
4 0 1 0.20 0 0
CUI: C1856285
Disease: Increased hepatic glycogen content
Increased hepatic glycogen content
4 0 1 0.20 0 0
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
4 0 1 0.20 0 0
Abnormality of endocrine pancreas physiology
4 0 1 0.20 0 0
Abnormality of the upper urinary tract
4 0 1 0.20 0 0