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: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
651 0 1 1.5E-03 0 0
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
Acute Undifferentiated Leukemia
119 0 2 1.6E-02 0 0
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
2235 0 1 4.5E-04 0 0
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
2438 0 1 4.1E-04 0 0
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
860 0 1 1.2E-03 0 0
Adult Acute Megakaryoblastic Leukemia
38 0 1 2.2E-02 0 0
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia
236 0 2 8.2E-03 0 0
CUI: C0278595
Disease: Adult Fibrosarcoma
Adult Fibrosarcoma
387 0 2 5.1E-03 0 0
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
2528 0 1 3.9E-04 0 0
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
1377 0 1 7.2E-04 0 0
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
405 0 1 2.4E-03 0 0
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
Adult Myelodysplastic Syndrome
332 0 3 8.9E-03 0 0
CUI: C0279070
Disease: Adult Oligodendroglioma
Adult Oligodendroglioma
154 0 1 6.2E-03 0 0
CUI: C0220613
Disease: Adult Soft Tissue Sarcoma
Adult Soft Tissue Sarcoma
162 0 1 5.9E-03 0 0
CUI: C0221056
Disease: Adult type dermatomyositis
Adult type dermatomyositis
218 0 1 4.4E-03 0 0
CUI: C4727838
Disease: Advanced Melanoma
Advanced Melanoma
73 0 1 1.2E-02 0 0
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
685 0 3 4.3E-03 0 0
Alcohol consumption during pregnancy
1 0 1 0.11 0 0
CUI: C3662483
Disease: Allergic sensitization
Allergic sensitization
85 0 1 1.1E-02 0 0
CUI: C0948201
Disease: Alloimmunisation
Alloimmunisation
65 0 2 2.8E-02 0 0
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome
51 0 3 5.3E-02 0 0
ALPORT SYNDROME 2, AUTOSOMAL RECESSIVE
4 0 2 0.18 0 0
ALPORT SYNDROME 3, AUTOSOMAL DOMINANT
3 43 2 0.20 1 2.3E-02
CUI: C1567743
Disease: Alport Syndrome, Autosomal Dominant
Alport Syndrome, Autosomal Dominant
5 0 1 7.7E-02 0 0
Alport Syndrome, Autosomal Recessive
8 0 1 6.2E-02 0 0