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: C0741796
Disease: Recurrent bronchitis
Recurrent bronchitis
29 0 11 0.14 0 0
CUI: C0747085
Disease: Recurrent otitis media
Recurrent otitis media
120 11 22 0.14 3 0.16
CUI: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia
76 0 16 0.13 0 0
CUI: C0007642
Disease: Cellulitis
Cellulitis
38 0 11 0.12 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection
69 0 14 0.12 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis
41 3 11 0.12 2 0.17
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood
75 0 14 0.11 0 0
CUI: C0009763
Disease: Conjunctivitis
Conjunctivitis
82 0 12 9.1E-02 0 0
CUI: C0025289
Disease: Meningitis
Meningitis
191 0 21 9.1E-02 0 0
Immunoglobulin Deficiency, Late-Onset
11 0 6 9.0E-02 0 0
CUI: C0037199
Disease: Sinusitis
Sinusitis
97 0 13 8.9E-02 0 0
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft
12 0 6 8.8E-02 0 0
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis
190 0 20 8.6E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia
43 0 8 8.2E-02 0 0
CUI: C0271441
Disease: Chronic otitis media
Chronic otitis media
163 0 17 8.2E-02 0 0
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis
121 14 13 7.6E-02 1 4.2E-02
Recurrent Staphylococcus aureus infections
11 0 5 7.4E-02 0 0
CUI: C4014733
Disease: Follicular hyperplasia
Follicular hyperplasia
11 0 5 7.4E-02 0 0
CUI: C1855067
Disease: B lymphocytopenia
B lymphocytopenia
13 0 5 7.1E-02 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
318 0 25 7.0E-02 0 0
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect
61 0 8 7.0E-02 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder
93 0 10 6.9E-02 0 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy
97 0 10 6.7E-02 0 0
CUI: C1860127
Disease: Impaired T cell function
Impaired T cell function
18 0 5 6.7E-02 0 0
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia
68 0 8 6.6E-02 0 0