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: C0545080
Disease: Composite Lymphoma
Composite Lymphoma
15 0 7 9.7E-02 0 0
CUI: C0020981
Disease: Angioimmunoblastic Lymphadenopathy
Angioimmunoblastic Lymphadenopathy
109 0 15 9.5E-02 0 0
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
42 0 9 9.3E-02 0 0
CUI: C3541994
Disease: Drug Hypersensitivity Syndrome
Drug Hypersensitivity Syndrome
43 0 9 9.2E-02 0 0
CUI: C4543948
Disease: Localized cutaneous leishmaniasis
Localized cutaneous leishmaniasis
20 0 7 9.1E-02 0 0
CUI: C0475801
Disease: Leukemia, Prolymphocytic, B-Cell
Leukemia, Prolymphocytic, B-Cell
23 0 7 8.7E-02 0 0
CUI: C0271429
Disease: Acute otitis media
Acute otitis media
24 0 7 8.6E-02 0 0
CUI: C0026766
Disease: Multiple Organ Failure
Multiple Organ Failure
25 0 7 8.5E-02 0 0
CUI: C4087124
Disease: Immunoglobulin G4-Related Disease
Immunoglobulin G4-Related Disease
80 0 11 8.3E-02 0 0
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia
162 0 17 8.1E-02 0 0
CUI: C0009812
Disease: Constitutional Symptom
Constitutional Symptom
30 0 7 8.0E-02 0 0
CUI: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma
124 0 14 8.0E-02 0 0
CUI: C3495801
Disease: Granulomatosis with polyangiitis
Granulomatosis with polyangiitis
126 0 14 8.0E-02 0 0
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies
211 0 20 7.8E-02 0 0
CUI: C0023443
Disease: Hairy Cell Leukemia
Hairy Cell Leukemia
143 0 15 7.8E-02 0 0
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma
76 0 10 7.7E-02 0 0
CUI: C1336753
Disease: Thyroid Lymphoma
Thyroid Lymphoma
20 0 6 7.7E-02 0 0
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection
21 0 6 7.6E-02 0 0
Chronic rejection of renal transplant
64 0 9 7.6E-02 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis
37 0 7 7.4E-02 0 0
Extranodal marginal zone B-cell lymphoma
23 0 6 7.4E-02 0 0
CUI: C0919746
Disease: Engraftment syndrome
Engraftment syndrome
9 0 5 7.4E-02 0 0
CUI: C0855139
Disease: Monocytoid B-cell lymphoma
Monocytoid B-cell lymphoma
24 0 6 7.3E-02 0 0
Anti-Basement Membrane Glomerulonephritis
39 0 7 7.3E-02 0 0
STRIATONIGRAL DEGENERATION, INFANTILE (disorder)
10 0 5 7.2E-02 0 0