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: C0522274
Disease: Humoral immune defect
Humoral immune defect
29 0 6 9.1E-02 0 0
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias
29 0 6 9.1E-02 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
89 0 11 9.1E-02 0 0
Chronic hepatitis due to cryptosporidium infection
5 0 4 9.1E-02 0 0
CUI: C4531154
Disease: Abnormal CD4:CD8 ratio
Abnormal CD4:CD8 ratio
5 0 4 9.1E-02 0 0
CUI: C0037023
Disease: Sialadenitis
Sialadenitis
42 0 7 9.0E-02 0 0
CUI: C1855781
Disease: Cutaneous anergy
Cutaneous anergy
6 0 4 8.9E-02 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder
93 0 11 8.8E-02 0 0
Decreased proportion of CD4-positive T cells
19 0 5 8.8E-02 0 0
CUI: C1849426
Disease: Lack of T cell function
Lack of T cell function
7 0 4 8.7E-02 0 0
CUI: C0021345
Disease: Infectious Mononucleosis
Infectious Mononucleosis
58 0 8 8.6E-02 0 0
CUI: C0745242
Disease: Immunoglobulin deficiency
Immunoglobulin deficiency
8 0 4 8.5E-02 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE
175 0 17 8.5E-02 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption
175 0 17 8.5E-02 0 0
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia
62 0 8 8.2E-02 0 0
Recurrent Staphylococcus aureus infections
11 0 4 8.0E-02 0 0
CUI: C1860128
Disease: Recurrent candida infections
Recurrent candida infections
12 0 4 7.8E-02 0 0
CUI: C0025289
Disease: Meningitis
Meningitis
191 0 17 7.8E-02 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome
95 0 10 7.8E-02 0 0
CUI: C1855067
Disease: B lymphocytopenia
B lymphocytopenia
13 0 4 7.7E-02 0 0
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency
86 0 9 7.5E-02 0 0
CUI: C0025309
Disease: Meningoencephalitis
Meningoencephalitis
30 0 5 7.4E-02 0 0
CUI: C0031350
Disease: Pharyngitis
Pharyngitis
30 0 5 7.4E-02 0 0
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome
45 0 6 7.3E-02 0 0
Selective immunoglobulin A deficiency
45 0 6 7.3E-02 0 0