Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Familial hyperchylomicronemia syndrome
5 0 2 0.25 0 0
CUI: C0853398
Disease: Endocarditis enterococcal
Endocarditis enterococcal
1 0 1 0.20 0 0
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
1 0 1 0.20 0 0
CUI: C4014767
Disease: HYPERLIPOPROTEINEMIA, TYPE ID
HYPERLIPOPROTEINEMIA, TYPE ID
1 9 1 0.20 2 0.15
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
1 0 1 0.20 0 0
HYPERTRIGLYCERIDEMIA, SUSCEPTIBILITY TO
1 0 1 0.20 0 0
CUI: C4025807
Disease: Atheroeruptive xanthoma
Atheroeruptive xanthoma
1 0 1 0.20 0 0
Hyperinsulinism due to HNF4A deficiency
1 0 1 0.20 0 0
Fatal post-viral neurodegenerative disorder
1 0 1 0.20 0 0
CUI: C0015938
Disease: Fetal Macrosomia
Fetal Macrosomia
2 0 1 0.17 0 0
CUI: C0271689
Disease: Insulin Receptor, Defect in
Insulin Receptor, Defect in
2 0 1 0.17 0 0
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism
2 0 1 0.17 0 0
CUI: C0851881
Disease: Enterococcal infection
Enterococcal infection
2 0 1 0.17 0 0
CUI: C1535978
Disease: Hyperchylomicronemia
Hyperchylomicronemia
2 0 1 0.17 0 0
CUI: C1856361
Disease: Doll-like facies
Doll-like facies
2 0 1 0.17 0 0
Idiopathic non-cirrhotic portal hypertension
2 0 1 0.17 0 0
CUI: C0020481
Disease: Hyperlipoproteinemia Type V
Hyperlipoproteinemia Type V
3 0 1 0.14 0 0
CUI: C1854704
Disease: Metabolic Ketosis
Metabolic Ketosis
3 0 1 0.14 0 0
Abnormality of exocrine pancreas physiology
3 0 1 0.14 0 0
Elevated gamma-glutamyltransferase activity
3 0 1 0.14 0 0
CUI: C0029002
Disease: Onchocerciasis, Ocular
Onchocerciasis, Ocular
4 0 1 0.12 0 0
CUI: C0339477
Disease: Lipidemia retinalis
Lipidemia retinalis
4 0 1 0.12 0 0
Maturity-Onset Diabetes of the Young, Type 1
4 24 1 0.12 1 3.4E-02
CUI: C1856285
Disease: Increased hepatic glycogen content
Increased hepatic glycogen content
4 0 1 0.12 0 0
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
4 0 1 0.12 0 0