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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 1.4E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.5E-02
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity
0 1 0 0 1 1.5E-02
CUI: C0241961
Disease: Angiomyolipoma of kidney
Angiomyolipoma of kidney
0 1 0 0 1 1.5E-02
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer
0 2 0 0 1 1.5E-02
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome
0 1 0 0 1 1.5E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.5E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.5E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.5E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.5E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.2E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
265 0 1 2.3E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 2.3E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 2.3E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.4E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 2.5E-03 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
225 0 1 2.5E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 1 2.5E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 2.5E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 2.5E-03 0 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
212 0 1 2.6E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 0 1 2.6E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 2.7E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy
190 0 1 2.7E-03 0 0