Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Philadelphia chromosome positive chronic myelogenous leukemia
27 0 9 0.18 0 0
Locally Advanced Squamous Cell Carcinoma
10 0 6 0.17 0 0
CUI: C0079746
Disease: Immunoblastic Large-Cell Lymphoma
Immunoblastic Large-Cell Lymphoma
28 0 7 0.13 0 0
Tuberculosis, Central Nervous System
11 0 5 0.13 0 0
Epstein-Barr virus associated gastric carcinoma
20 0 6 0.13 0 0
CUI: C0400807
Disease: Stress ulcer of stomach
Stress ulcer of stomach
14 0 5 0.12 0 0
CUI: C2741638
Disease: Stress ulcer
Stress ulcer
14 0 5 0.12 0 0
CUI: C0302360
Disease: Disease caused by Shigella boydii
Disease caused by Shigella boydii
5 0 4 0.12 0 0
CUI: C1394254
Disease: Cryptitis
Cryptitis
5 0 4 0.12 0 0
Human T-cell lymphotrophic virus, type I [HTLV-I]
25 0 6 0.12 0 0
CUI: C4289581
Disease: RELA fusion-positive ependymoma
RELA fusion-positive ependymoma
6 0 4 0.12 0 0
CUI: C0023486
Disease: Prolymphocytic Leukemia
Prolymphocytic Leukemia
37 0 7 0.11 0 0
CUI: C4528176
Disease: High Risk Myelodysplastic Syndrome
High Risk Myelodysplastic Syndrome
19 0 5 0.11 0 0
CUI: C0006285
Disease: Bronchopneumonia
Bronchopneumonia
9 0 4 0.11 0 0
CUI: C0154652
Disease: Eosinophilic meningitis
Eosinophilic meningitis
9 0 4 0.11 0 0
Aggressive natural killer-cell leukemia
30 0 6 0.11 0 0
CUI: C1959584
Disease: Cardiac Carcinoma
Cardiac Carcinoma
10 0 4 0.11 0 0
CUI: C1301797
Disease: Induced hypothermia (finding)
Induced hypothermia (finding)
21 0 5 0.10 0 0
CUI: C0349637
Disease: Common acute lymphoblastic leukemia
Common acute lymphoblastic leukemia
43 0 7 0.10 0 0
CUI: C0023464
Disease: Acute biphenotypic leukemia
Acute biphenotypic leukemia
45 0 7 1.0E-01 0 0
CUI: C0432411
Disease: Chromosome 9, trisomy
Chromosome 9, trisomy
12 0 4 1.0E-01 0 0
CUI: C0349532
Disease: Gastric lymphoma
Gastric lymphoma
24 0 5 9.8E-02 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy
24 0 5 9.8E-02 0 0
CUI: C0030779
Disease: Pelger-Huet Anomaly
Pelger-Huet Anomaly
25 0 5 9.6E-02 0 0
CUI: C0022972
Disease: Lambert-Eaton Myasthenic Syndrome
Lambert-Eaton Myasthenic Syndrome
37 0 6 9.5E-02 0 0