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: C4023452
Disease: Elevated C-reactive protein level
Elevated C-reactive protein level 		28 0 5 8.3E-02 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		42 0 6 8.2E-02 0 0
CUI: C1843139
Disease: Hypercholanemia, Familial
Hypercholanemia, Familial 		3 0 3 8.1E-02 0 0
CUI: C1850083
Disease: Irregular ossification at anterior rib ends
Irregular ossification at anterior rib ends 		3 0 3 8.1E-02 0 0
CUI: C1859162
Disease: Neonatal cholestatic liver disease
Neonatal cholestatic liver disease 		3 0 3 8.1E-02 0 0
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		3 0 3 8.1E-02 0 0
CUI: C0341471
Disease: Idiopathic chronic pancreatitis
Idiopathic chronic pancreatitis 		17 0 4 8.0E-02 0 0
CUI: C1853564
Disease: Developmental Delay, Epilepsy, and Neonatal Diabetes
Developmental Delay, Epilepsy, and Neonatal Diabetes 		4 0 3 7.9E-02 0 0
CUI: C0267937
Disease: Acute recurrent pancreatitis
Acute recurrent pancreatitis 		18 0 4 7.8E-02 0 0
CUI: C4023004
Disease: Increased serum bile acid concentration
Increased serum bile acid concentration 		5 0 3 7.7E-02 0 0
CUI: C0266267
Disease: Congenital hypoplasia of pancreas
Congenital hypoplasia of pancreas 		20 0 4 7.5E-02 0 0
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		20 0 4 7.5E-02 0 0
CUI: C2675627
Disease: Acholic stool
Acholic stool 		6 0 3 7.5E-02 0 0
CUI: C1836320
Disease: Proximal femoral metaphyseal irregularity
Proximal femoral metaphyseal irregularity 		7 0 3 7.3E-02 0 0
CUI: C1850087
Disease: Narrow sacroiliac notch
Narrow sacroiliac notch 		7 0 3 7.3E-02 0 0
CUI: C1856904
Disease: Reduced pancreatic beta cells
Reduced pancreatic beta cells 		7 0 3 7.3E-02 0 0
CUI: C3552526
Disease: Metaphyseal sclerosis
Metaphyseal sclerosis 		7 0 3 7.3E-02 0 0
CUI: C0017979
Disease: Glycosuria
Glycosuria 		53 0 6 7.1E-02 0 0
CUI: C1857180
Disease: Enlargement of the costochondral junction
Enlargement of the costochondral junction 		8 0 3 7.1E-02 0 0
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis 		54 0 6 7.1E-02 0 0
CUI: C1857949
Disease: Prominent metopic ridge
Prominent metopic ridge 		39 0 5 7.0E-02 0 0
CUI: C0028961
Disease: Oliguria
Oliguria 		24 0 4 7.0E-02 0 0
CUI: C0239941
Disease: Persistence of hemoglobin F
Persistence of hemoglobin F 		9 0 3 7.0E-02 0 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase 		212 0 16 6.9E-02 0 0
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		10 0 3 6.8E-02 0 0