Source: ALL
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: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia 		76 0 23 0.18 0 0
CUI: C2936665
Disease: Immunoglobulin Deficiency, Late-Onset
Immunoglobulin Deficiency, Late-Onset 		11 0 11 0.15 0 0
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft 		12 0 11 0.14 0 0
CUI: C0741796
Disease: Recurrent bronchitis
Recurrent bronchitis 		29 0 12 0.13 0 0
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency 		86 0 17 0.12 0 0
CUI: C0024312
Disease: Lymphopenia
Lymphopenia 		239 16 33 0.12 1 5.0E-02
CUI: C0013990
Disease: Pathological accumulation of air in tissues
Pathological accumulation of air in tissues 		69 0 15 0.12 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection 		69 0 15 0.12 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 17 0.12 0 0
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia 		62 0 14 0.11 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder 		93 0 17 0.11 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 24 0.11 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 24 0.11 0 0
CUI: C3277226
Disease: Restrictive ventilatory defect
Restrictive ventilatory defect 		61 0 13 0.11 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections 		318 7 36 0.10 1 9.1E-02
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy 		277 0 32 1.0E-01 0 0
CUI: C0239998
Disease: Recurrent infections
Recurrent infections 		127 0 18 9.8E-02 0 0
CUI: C0034150
Disease: Purpura
Purpura 		68 0 12 9.2E-02 0 0
CUI: C0038002
Disease: Splenomegaly
Splenomegaly 		345 0 35 9.1E-02 0 0
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis 		190 0 21 8.6E-02 0 0
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		207 0 22 8.5E-02 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome 		239 0 24 8.3E-02 0 0
CUI: C1855204
Disease: Cellular immunodeficiency
Cellular immunodeficiency 		30 0 8 8.2E-02 0 0
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 0 16 7.5E-02 0 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy 		97 0 12 7.5E-02 0 0