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: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 3.3E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 1 3.0E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis
0 1 0 0 1 3.3E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 3.3E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania
0 1 0 0 1 3.3E-03
CUI: C0700299
Disease: Heinz Body Anemias
Heinz Body Anemias
0 19 0 0 1 3.1E-03
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1
0 20 0 0 1 3.1E-03
Beta Thalassemia, Dominant Inclusion Body Type
0 14 0 0 1 3.1E-03
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 3.3E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 3.3E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.2E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.3E-03
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 3.2E-03
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 3.3E-03
Frequent episodic tension-type headache
0 1 0 0 1 3.3E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 6.5E-03
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute
2 0 1 9.3E-04 0 0
CUI: C0000729
Disease: Abdominal Cramps
Abdominal Cramps
1 0 1 9.3E-04 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced
5 0 1 9.3E-04 0 0
CUI: C0000921
Disease: Accidental Falls
Accidental Falls
22 0 1 9.1E-04 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 9.3E-04 0 0
Herpetic Acute Necrotizing Encephalitis
5 0 1 9.3E-04 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis
2 0 1 9.3E-04 0 0
CUI: C0001630
Disease: Adrenal Rest Tumor
Adrenal Rest Tumor
2 0 1 9.3E-04 0 0
CUI: C0001733
Disease: Afibrinogenemia
Afibrinogenemia
9 0 1 9.2E-04 0 0