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: C0039730
Disease: Thalassemia
Thalassemia 		136 18 9 6.0E-02 2 0.11
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 3 5 0.12 2 0.50
CUI: C0271979
Disease: Thalassemia Intermedia
Thalassemia Intermedia 		53 8 7 0.10 2 0.22
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 25 3 1.9E-02 1 3.7E-02
CUI: C0001546
Disease: Adjustment Disorders
Adjustment Disorders 		9 4 1 3.3E-02 1 0.17
CUI: C0001815
Disease: Primary Myelofibrosis
Primary Myelofibrosis 		282 29 3 1.0E-02 1 3.2E-02
CUI: C0002871
Disease: Anemia
Anemia 		847 94 17 2.0E-02 1 1.0E-02
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 1 1 4.5E-02 1 0.33
CUI: C0002893
Disease: Refractory anemias
Refractory anemias 		340 11 3 8.4E-03 1 7.7E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		502 243 1 1.9E-03 1 4.1E-03
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		198 103 11 5.3E-02 1 9.5E-03
CUI: C0005699
Disease: Blast Phase
Blast Phase 		299 14 3 9.4E-03 1 6.2E-02
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		267 31 2 7.0E-03 1 3.0E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		6941 3417 12 1.7E-03 1 2.9E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		8621 1641 14 1.6E-03 1 6.1E-04
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		3926 712 8 2.0E-03 1 1.4E-03
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		757 47 3 3.9E-03 1 2.0E-02
CUI: C0009812
Disease: Constitutional Symptom
Constitutional Symptom 		30 1 1 2.0E-02 1 0.33
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		1282 440 10 7.7E-03 1 2.3E-03
CUI: C0014122
Disease: Subacute Bacterial Endocarditis
Subacute Bacterial Endocarditis 		12 1 1 3.0E-02 1 0.33
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		325 23 1 2.9E-03 1 4.0E-02
CUI: C0014518
Disease: Toxic Epidermal Necrolysis
Toxic Epidermal Necrolysis 		143 29 1 6.1E-03 1 3.2E-02
CUI: C0014804
Disease: Erythromelalgia
Erythromelalgia 		14 5 1 2.9E-02 1 0.14
CUI: C0017925
Disease: Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VI 		15 22 1 2.8E-02 1 4.2E-02
CUI: C0018939
Disease: Hematological Disease
Hematological Disease 		255 16 7 2.6E-02 1 5.6E-02