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: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		194 269 51 0.26 16 5.9E-02
CUI: C0270210
Disease: Lucey-Driscoll syndrome (disorder)
Lucey-Driscoll syndrome (disorder) 		9 0 9 0.18 0 0
CUI: C1866173
Disease: BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1 		9 0 9 0.18 0 0
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
Crigler Najjar syndrome, type 2 		9 0 9 0.18 0 0
CUI: C4303163
Disease: Autoimmune hepatitis type 2
Autoimmune hepatitis type 2 		16 0 10 0.18 0 0
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
Crigler Najjar syndrome, type 1 		17 0 10 0.17 0 0
CUI: C0741494
Disease: Elevated total bilirubin
Elevated total bilirubin 		17 0 10 0.17 0 0
CUI: C0311468
Disease: Increased bilirubin level (finding)
Increased bilirubin level (finding) 		14 0 9 0.16 0 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia 		23 0 10 0.16 0 0
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		33 0 10 0.14 0 0
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder) 		40 0 10 0.12 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 9 0.12 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 7 0.12 0 0
CUI: C0342753
Disease: Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogen storage disease due to acid maltase deficiency, late-onset 		8 0 6 0.11 0 0
CUI: C4755308
Disease: Familial cervical artery dissection
Familial cervical artery dissection 		9 0 6 0.11 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		143 0 19 0.11 0 0
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 0 10 0.11 0 0
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		108 0 15 0.10 0 0
CUI: C0022610
Disease: Kernicterus
Kernicterus 		17 0 6 9.7E-02 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		63 16 10 9.6E-02 1 3.2E-02
CUI: C3888924
Disease: Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, infantile onset 		7 6 5 9.4E-02 2 1.0E-01
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		67 0 10 9.3E-02 0 0
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		56 0 9 9.2E-02 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases 		130 0 15 9.0E-02 0 0
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		70 0 10 9.0E-02 0 0