Source: ALL
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: C0151747
Disease: Renal tubular disorder
Renal tubular disorder 		64 0 9 0.11 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 3 0.11 0 0
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia 		5 0 3 0.11 0 0
CUI: C0497406
Disease: Overweight
Overweight 		27 0 5 0.10 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 9 0.10 0 0
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		30 0 5 9.8E-02 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 4 9.8E-02 0 0
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		8 0 3 9.7E-02 0 0
CUI: C0158986
Disease: Neonatal hypoglycemia
Neonatal hypoglycemia 		55 0 7 9.5E-02 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		102 0 11 9.4E-02 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		10 0 3 9.1E-02 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system 		34 0 5 9.1E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 9 8.8E-02 0 0
CUI: C2748055
Disease: Hypoinsulinaemia (disorder)
Hypoinsulinaemia (disorder) 		36 0 5 8.8E-02 0 0
CUI: C0038238
Disease: Steatorrhea
Steatorrhea 		37 0 5 8.6E-02 0 0
CUI: C0027773
Disease: Nesidioblastosis
Nesidioblastosis 		12 0 3 8.6E-02 0 0
CUI: C0597167
Disease: Islets of Langerhans hyperplasia
Islets of Langerhans hyperplasia 		12 0 3 8.6E-02 0 0
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia 		52 0 6 8.3E-02 0 0
CUI: C4703555
Disease: Decreased waist to hip ratio
Decreased waist to hip ratio 		28 0 4 8.0E-02 0 0
CUI: C1836189
Disease: Radial deviation of finger
Radial deviation of finger 		42 0 5 7.9E-02 0 0
CUI: C0271713
Disease: Ketotic hypoglycemia
Ketotic hypoglycemia 		15 0 3 7.9E-02 0 0
CUI: C1856438
Disease: Hypoketotic hypoglycemia
Hypoketotic hypoglycemia 		15 0 3 7.9E-02 0 0
CUI: C1848395
Disease: Large for gestational age
Large for gestational age 		43 0 5 7.8E-02 0 0
CUI: C0342720
Disease: Adenosylcobalamin synthesis defect
Adenosylcobalamin synthesis defect 		2 0 2 7.7E-02 0 0
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		2 0 2 7.7E-02 0 0