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 1.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.3E-02
CUI: C0162316
Disease: Iron deficiency anemia
Iron deficiency anemia
0 21 0 0 1 1.0E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism
0 5 0 0 2 2.5E-02
CUI: C0392514
Disease: Hereditary hemochromatosis
Hereditary hemochromatosis
0 56 0 0 1 7.5E-03
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome
0 144 0 0 1 4.5E-03
CUI: C0919890
Disease: Hyperfibrinogenemia
Hyperfibrinogenemia
0 1 0 0 1 1.3E-02
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome
0 21 0 0 2 2.1E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
0 13 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.3E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.3E-02
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
0 2 0 0 1 1.3E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 1.3E-02
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 1.6E-02 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden
1 0 1 1.6E-02 0 0
CUI: C0020683
Disease: Hypovolemic Shock
Hypovolemic Shock
1 0 1 1.6E-02 0 0
CUI: C0021177
Disease: Increased Libido
Increased Libido
1 0 1 1.6E-02 0 0
Other specified hemorrhagic conditions
1 0 1 1.6E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus
1 0 1 1.6E-02 0 0
CUI: C0085697
Disease: Chronic pyelonephritis
Chronic pyelonephritis
1 0 1 1.6E-02 0 0
Malignant neoplasm of superior wall of nasopharynx
1 0 1 1.6E-02 0 0
Malignant tumor of posterior wall of nasopharynx
1 0 1 1.6E-02 0 0
Malignant tumor of lateral wall of nasopharynx
1 0 1 1.6E-02 0 0
Malignant tumor of anterior wall of nasopharynx
1 0 1 1.6E-02 0 0
CUI: C0154695
Disease: Diplegic Infantile Cerebral Palsy
Diplegic Infantile Cerebral Palsy
1 0 1 1.6E-02 0 0