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: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 8 8.2E-02 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 8 8.2E-02 0 0
CUI: C0887850
Disease: Polycystic Kidney, Type 1 Autosomal Dominant Disease
Polycystic Kidney, Type 1 Autosomal Dominant Disease 		10 0 2 8.0E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst 		26 0 3 7.5E-02 0 0
CUI: C2939465
Disease: Deficiency of glucose-6-phosphate dehydrogenase
Deficiency of glucose-6-phosphate dehydrogenase 		75 0 6 7.0E-02 0 0
CUI: C0002875
Disease: Cooley's anemia
Cooley's anemia 		144 0 10 6.6E-02 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		131 0 9 6.5E-02 0 0
CUI: C0002312
Disease: alpha-Thalassemia
alpha-Thalassemia 		86 0 6 6.2E-02 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		143 0 9 6.0E-02 0 0
CUI: C0268309
Disease: Inherited disorder of bilirubin metabolism
Inherited disorder of bilirubin metabolism 		1 0 1 5.9E-02 0 0
CUI: C0338329
Disease: recurrent childhood brain stem glioma
recurrent childhood brain stem glioma 		1 0 1 5.9E-02 0 0
CUI: C0432273
Disease: Worth disease
Worth disease 		1 0 1 5.9E-02 0 0
CUI: C0473118
Disease: Physiological hyperbilirubinemia (disorder)
Physiological hyperbilirubinemia (disorder) 		1 0 1 5.9E-02 0 0
CUI: C0853398
Disease: Endocarditis enterococcal
Endocarditis enterococcal 		1 0 1 5.9E-02 0 0
CUI: C1531394
Disease: Perinatal jaundice
Perinatal jaundice 		1 0 1 5.9E-02 0 0
CUI: C1833508
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 		1 0 1 5.9E-02 0 0
CUI: C1833511
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE 		1 0 1 5.9E-02 0 0
CUI: C1833518
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 		1 0 1 5.9E-02 0 0
CUI: C1837273
Disease: Long-chain dicarboxylic aciduria
Long-chain dicarboxylic aciduria 		1 0 1 5.9E-02 0 0
CUI: C1840419
Disease: Metacarpal diaphyseal endosteal sclerosis
Metacarpal diaphyseal endosteal sclerosis 		1 0 1 5.9E-02 0 0
CUI: C1840420
Disease: Metatarsal diaphyseal endosteal sclerosis
Metatarsal diaphyseal endosteal sclerosis 		1 0 1 5.9E-02 0 0
CUI: C1842154
Disease: Sclerotic vertebral body
Sclerotic vertebral body 		1 0 1 5.9E-02 0 0
CUI: C1843323
Disease: Van Buchem disease type 2
Van Buchem disease type 2 		1 0 1 5.9E-02 0 0
CUI: C1843330
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
OSTEOPETROSIS, AUTOSOMAL DOMINANT 1 		1 0 1 5.9E-02 0 0
CUI: C1864668
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 		1 0 1 5.9E-02 0 0