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: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome
31 0 1 2.9E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 1 0.12 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.3E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology
35 0 1 2.6E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 5.0E-03 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.7E-03 0 0
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
56 0 1 1.7E-02 0 0
CUI: C0392609
Disease: Acquired hypofibrinogenemia
Acquired hypofibrinogenemia
1 0 1 0.25 0 0
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
639 0 1 1.6E-03 0 0
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
1293 0 1 7.7E-04 0 0
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis
435 0 1 2.3E-03 0 0
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
651 0 1 1.5E-03 0 0
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
656 0 1 1.5E-03 0 0
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
860 0 1 1.2E-03 0 0
CUI: C0278764
Disease: Adult Burkitt Lymphoma
Adult Burkitt Lymphoma
475 0 1 2.1E-03 0 0
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
2528 0 2 7.9E-04 0 0
CUI: C0278721
Disease: Adult Lymphoblastic Lymphoma
Adult Lymphoblastic Lymphoma
85 0 1 1.1E-02 0 0
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
1169 0 1 8.5E-04 0 0
CUI: C0278876
Disease: Adult Medulloblastoma
Adult Medulloblastoma
762 0 1 1.3E-03 0 0
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
370 0 1 2.7E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 2 1.1E-02 0 0
CUI: C0001824
Disease: Agranulocytosis
Agranulocytosis
55 0 1 1.7E-02 0 0
CUI: C0523459
Disease: Alanine measurement
Alanine measurement
3 3 2 0.40 2 0.25
Amino Acid Metabolism, Inborn Errors
20 0 2 9.1E-02 0 0