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: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology 		3 0 3 9.4E-02 0 0
CUI: C2981142
Disease: Refractory anemia, without ringed sideroblasts, without excess blasts
Refractory anemia, without ringed sideroblasts, without excess blasts 		38 2 6 9.4E-02 1 0.17
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		15 2 4 9.3E-02 1 0.17
CUI: C0279543
Disease: Philadelphia chromosome positive chronic myelogenous leukemia
Philadelphia chromosome positive chronic myelogenous leukemia 		27 0 5 9.3E-02 0 0
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		158 28 16 9.2E-02 2 6.5E-02
CUI: C0271987
Disease: ^A^gamma delta beta^0^ thalassemia
^A^gamma delta beta^0^ thalassemia 		4 0 3 9.1E-02 0 0
CUI: C0585216
Disease: Alpha-Thalassemia Myelodysplasia Syndrome
Alpha-Thalassemia Myelodysplasia Syndrome 		4 0 3 9.1E-02 0 0
CUI: C0850672
Disease: hereditary anemia
hereditary anemia 		4 0 3 9.1E-02 0 0
CUI: C1268964
Disease: Myelodysplastic syndrome, no ICD-O subtype
Myelodysplastic syndrome, no ICD-O subtype 		4 0 3 9.1E-02 0 0
CUI: C1292771
Disease: Chronic myelogenous leukemia, BCR/ABL positive
Chronic myelogenous leukemia, BCR/ABL positive 		4 0 3 9.1E-02 0 0
CUI: C2347507
Disease: Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
Childhood B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 		4 0 3 9.1E-02 0 0
CUI: C3150773
Disease: CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME
CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME 		17 0 4 8.9E-02 0 0
CUI: C0239574
Disease: Low grade fever
Low grade fever 		5 0 3 8.8E-02 0 0
CUI: C1275661
Disease: Acute myeloid leukemia with recurrent genetic abnormality
Acute myeloid leukemia with recurrent genetic abnormality 		5 0 3 8.8E-02 0 0
CUI: C3539063
Disease: Bart's Hemoglobinopathy
Bart's Hemoglobinopathy 		5 0 3 8.8E-02 0 0
CUI: C4274391
Disease: Dominant beta-thalassemia
Dominant beta-thalassemia 		5 0 3 8.8E-02 0 0
CUI: C0206141
Disease: Idiopathic Hypereosinophilic Syndrome
Idiopathic Hypereosinophilic Syndrome 		43 5 6 8.7E-02 1 0.11
CUI: C0221013
Disease: Mastocytosis, Systemic
Mastocytosis, Systemic 		94 11 10 8.6E-02 1 6.7E-02
CUI: C0016199
Disease: Flank Pain
Flank Pain 		6 0 3 8.6E-02 0 0
CUI: C0032461
Disease: Polycythemia
Polycythemia 		82 22 9 8.6E-02 1 3.8E-02
CUI: C0553699
Disease: Heinz body observation
Heinz body observation 		6 0 3 8.6E-02 0 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement 		6 0 3 8.6E-02 0 0
CUI: C0221019
Disease: Sickle cell-beta-thalassemia
Sickle cell-beta-thalassemia 		7 0 3 8.3E-02 0 0
CUI: C0271990
Disease: delta-Thalassemia
delta-Thalassemia 		7 0 3 8.3E-02 0 0
CUI: C4025187
Disease: Increased megakaryocyte count
Increased megakaryocyte count 		7 0 3 8.3E-02 0 0