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: C0702266
Disease: Basophilia
Basophilia
12 0 2 0.17 0 0
CUI: C1112746
Disease: Hepatic lymphoma
Hepatic lymphoma
5 0 1 0.17 0 0
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
12 0 2 0.17 0 0
CUI: C2347753
Disease: Adult Pure Erythroid Leukemia
Adult Pure Erythroid Leukemia
5 0 1 0.17 0 0
CUI: C4023028
Disease: Granulocytic hyperplasia
Granulocytic hyperplasia
5 0 1 0.17 0 0
CUI: C0476486
Disease: Generalized enlarged lymph nodes
Generalized enlarged lymph nodes
13 0 2 0.15 0 0
CUI: C0023488
Disease: Leukemia, Radiation-Induced
Leukemia, Radiation-Induced
6 0 1 0.14 0 0
Papillary renal cell carcinoma type 2
6 0 1 0.14 0 0
CUI: C1866806
Disease: Unilateral ptosis
Unilateral ptosis
6 0 1 0.14 0 0
Infant Acute Undifferentiated Leukemia
14 0 2 0.14 0 0
CUI: C4707057
Disease: Tetrasomy 21
Tetrasomy 21
6 0 1 0.14 0 0
CUI: C1282609
Disease: Granulocytosis
Granulocytosis
15 0 2 0.13 0 0
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis
15 0 2 0.13 0 0
CUI: C0023481
Disease: Chronic Neutrophilic Leukemia
Chronic Neutrophilic Leukemia
16 0 2 0.12 0 0
Autosomal recessive agammaglobulinemia
7 0 1 0.12 0 0
Lymphoepithelioid lymphoma (clinical)
7 0 1 0.12 0 0
Acute lymphoblastic leukemia with lymphomatous features
7 0 1 0.12 0 0
Chronic myeloid leukemia, BCR/ABL-positive
7 0 1 0.12 0 0
CUI: C4303761
Disease: Familial thrombocytosis
Familial thrombocytosis
7 0 1 0.12 0 0
CUI: C0546968
Disease: Fistula of branchial cleft
Fistula of branchial cleft
8 0 1 0.11 0 0
Myeloproliferative Neoplasm, Unclassifiable
8 0 1 0.11 0 0
CUI: C1845247
Disease: Indolence
Indolence
8 0 1 0.11 0 0
CUI: C0685898
Disease: Food anaphylaxis
Food anaphylaxis
9 0 1 1.0E-01 0 0
CUI: C4021808
Disease: Abnormality of earlobe
Abnormality of earlobe
9 0 1 1.0E-01 0 0
CUI: C0279582
Disease: Childhood Burkitt Leukemia
Childhood Burkitt Leukemia
10 0 1 9.1E-02 0 0