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 69 0.11 0 0
Epidermolysis Bullosa Simplex Superficialis
11 0 6 8.0E-02 0 0
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency
56 0 9 7.7E-02 0 0
CUI: C0521858
Disease: Decreased drug resistance
Decreased drug resistance
15 0 6 7.6E-02 0 0
CUI: C0272401
Disease: Virchow's node (disorder)
Virchow's node (disorder)
30 0 7 7.5E-02 0 0
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia
60 0 9 7.4E-02 0 0
CUI: C4022608
Disease: Oral cavity bleeding
Oral cavity bleeding
18 0 6 7.3E-02 0 0
Leukoencephalopathy, Progressive Multifocal
240 0 21 7.3E-02 0 0
High-Grade Prostatic Intraepithelial Neoplasia
111 0 12 7.1E-02 0 0
Gastroparesis with diabetes mellitus
21 0 6 7.1E-02 0 0
CUI: C0263661
Disease: Disorder of skeletal system
Disorder of skeletal system
25 0 6 6.7E-02 0 0
CUI: C0013491
Disease: Ecchymosis
Ecchymosis
41 0 7 6.7E-02 0 0
CUI: C1860320
Disease: Bone marrow hypercellularity
Bone marrow hypercellularity
26 0 6 6.7E-02 0 0
CUI: C3267047
Disease: Autoimmune necrotizing myopathy
Autoimmune necrotizing myopathy
11 0 5 6.6E-02 0 0
CUI: C0085253
Disease: Adult-Onset Still Disease
Adult-Onset Still Disease
76 0 9 6.6E-02 0 0
CUI: C0340279
Disease: Ventricular hypertrophy
Ventricular hypertrophy
60 0 8 6.6E-02 0 0
CUI: C2745900
Disease: Promyelocytic leukemia
Promyelocytic leukemia
255 0 20 6.6E-02 0 0
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy
28 0 6 6.5E-02 0 0
Neuronal intranuclear inclusion disease
12 0 5 6.5E-02 0 0
CUI: C0206693
Disease: Medullary carcinoma
Medullary carcinoma
81 0 9 6.3E-02 0 0
CUI: C0206631
Disease: Lipomatous neoplasm
Lipomatous neoplasm
14 0 5 6.3E-02 0 0
CUI: C0333440
Disease: Hyaline body
Hyaline body
14 0 5 6.3E-02 0 0
CUI: C0221032
Disease: Familial generalized lipodystrophy
Familial generalized lipodystrophy
49 0 7 6.2E-02 0 0
CUI: C1368019
Disease: Paget Disease
Paget Disease
66 0 8 6.2E-02 0 0
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage
50 0 7 6.2E-02 0 0