Source: ALL
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: C0015967
Disease: Fever
Fever 		1021 66 139 0.11 1 6.2E-03
CUI: C0024312
Disease: Lymphopenia
Lymphopenia 		239 16 61 0.11 2 1.8E-02
CUI: C0023518
Disease: Leukocytosis
Leukocytosis 		168 0 54 0.11 0 0
CUI: C0038362
Disease: Stomatitis
Stomatitis 		109 22 48 0.11 3 2.6E-02
CUI: C0023895
Disease: Liver diseases
Liver diseases 		1019 100 135 0.11 1 5.1E-03
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
Adult Myelodysplastic Syndrome 		332 20 69 0.11 5 4.5E-02
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease 		447 25 80 0.11 1 8.3E-03
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
Childhood Myelodysplastic Syndrome 		335 20 69 0.11 5 4.5E-02
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma 		399 27 75 0.11 5 4.2E-02
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		1293 222 160 0.11 11 3.6E-02
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		900 148 122 0.10 6 2.5E-02
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		1169 66 147 0.10 6 3.8E-02
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma 		1171 66 147 0.10 6 3.8E-02
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 65 0.10 0 0
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		430 80 77 0.10 3 1.7E-02
CUI: C0015230
Disease: Exanthema
Exanthema 		251 14 60 0.10 1 9.1E-03
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		1172 115 146 0.10 14 7.1E-02
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE 		350 19 69 0.10 1 8.7E-03
CUI: C0032463
Disease: Polycythemia Vera
Polycythemia Vera 		291 38 63 0.10 1 7.5E-03
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma 		399 29 73 0.10 5 4.1E-02
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular 		477 83 80 0.10 4 2.3E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		502 243 82 0.10 4 1.2E-02
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		757 47 105 0.10 6 4.3E-02
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
Malignant neoplasm of gastrointestinal tract 		423 55 74 0.10 1 6.6E-03
CUI: C0019158
Disease: Hepatitis
Hepatitis 		656 42 95 1.0E-01 4 3.0E-02