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: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders
267 0 1 3.7E-03 0 0
CUI: C0007097
Disease: Carcinoma
Carcinoma
2462 0 1 4.1E-04 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis
420 0 2 4.8E-03 0 0
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis
54 0 2 3.7E-02 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
5473 0 1 1.8E-04 0 0
Diabetes Mellitus, Non-Insulin-Dependent
3134 0 1 3.2E-04 0 0
CUI: C0011991
Disease: Diarrhea
Diarrhea
632 0 1 1.6E-03 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
842 0 2 2.4E-03 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia
88 0 1 1.1E-02 0 0
CUI: C0017181
Disease: Gastrointestinal Hemorrhage
Gastrointestinal Hemorrhage
122 0 1 8.1E-03 0 0
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
523 0 1 1.9E-03 0 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
131 0 1 7.6E-03 0 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
2322 0 1 4.3E-04 0 0
CUI: C0020541
Disease: Portal Hypertension
Portal Hypertension
167 0 1 6.0E-03 0 0
CUI: C0022346
Disease: Icterus
Icterus
241 0 1 4.1E-03 0 0
CUI: C0023418
Disease: leukemia
leukemia
2111 0 1 4.7E-04 0 0
CUI: C0023895
Disease: Liver diseases
Liver diseases
1019 0 1 9.8E-04 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome
239 0 1 4.2E-03 0 0
CUI: C0027092
Disease: Myopia
Myopia
490 0 1 2.0E-03 0 0
CUI: C0027613
Disease: Neonatal hepatitis
Neonatal hepatitis
21 0 1 4.5E-02 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms
10161 0 2 2.0E-04 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 5.9E-03 0 0
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
1098 0 1 9.1E-04 0 0
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
2078 0 1 4.8E-04 0 0
CUI: C0033774
Disease: Pruritus
Pruritus
107 0 2 1.9E-02 0 0