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: C0205854
Disease: Glandular Neoplasms
Glandular Neoplasms
8 0 2 0.15 0 0
CUI: C0266785
Disease: Abnormal umbilical cord
Abnormal umbilical cord
1 0 1 0.14 0 0
CUI: C0302874
Disease: Depressive personality disorder
Depressive personality disorder
1 0 1 0.14 0 0
CUI: C0749098
Disease: Hematoma, Subdural, Acute
Hematoma, Subdural, Acute
1 0 1 0.14 0 0
CUI: C0751797
Disease: Intracranial Hematoma, Traumatic
Intracranial Hematoma, Traumatic
1 0 1 0.14 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome
1 0 1 0.14 0 0
CUI: C0020640
Disease: Inherited Factor II deficiency
Inherited Factor II deficiency
2 0 1 0.12 0 0
Purine-Pyrimidine Metabolism, Inborn Errors
2 0 1 0.12 0 0
CUI: C0274576
Disease: Poisoning by fluorouracil
Poisoning by fluorouracil
2 0 1 0.12 0 0
CUI: C0750325
Disease: Vomiting, recurrent
Vomiting, recurrent
2 0 1 0.12 0 0
Reduced dihydropyrimidine dehydrogenase activity
2 0 1 0.12 0 0
Hereditary factor VIII deficiency disease with inhibitor
3 0 1 0.11 0 0
CUI: C0476270
Disease: Cardiovascular symptoms
Cardiovascular symptoms
3 0 1 0.11 0 0
CUI: C1848657
Disease: Long ear
Long ear
3 0 1 0.11 0 0
CUI: C3495551
Disease: Dihydropyrimidinuria
Dihydropyrimidinuria
3 0 1 0.11 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis
3 0 1 0.11 0 0
CUI: C4024722
Disease: Reduced factor VII activity
Reduced factor VII activity
4 0 1 1.0E-01 0 0
CUI: C0278502
Disease: recurrent gastric cancer
recurrent gastric cancer
16 0 2 9.5E-02 0 0
CUI: C0032787
Disease: Postoperative Complications
Postoperative Complications
5 0 1 9.1E-02 0 0
CUI: C0751893
Disease: Posterior Fossa Hemorrhage
Posterior Fossa Hemorrhage
5 0 1 9.1E-02 0 0
CUI: C0032797
Disease: Postpartum Hemorrhage
Postpartum Hemorrhage
6 0 1 8.3E-02 0 0
CUI: C0036224
Disease: Sarcoma, Yoshida
Sarcoma, Yoshida
6 0 1 8.3E-02 0 0
CUI: C0240412
Disease: Muscle hematoma
Muscle hematoma
6 0 1 8.3E-02 0 0
Dihydropyrimidine Dehydrogenase Deficiency
7 0 1 7.7E-02 0 0
CUI: C0020435
Disease: Hyperbilirubinemia, Hereditary
Hyperbilirubinemia, Hereditary
8 0 1 7.1E-02 0 0