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: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 21 0.26 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 21 0.23 0 0
CUI: C1844384
Disease: Recurrent fungal infections
Recurrent fungal infections 		20 0 13 0.17 0 0
CUI: C0009763
Disease: Conjunctivitis
Conjunctivitis 		82 0 20 0.15 0 0
CUI: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia 		76 0 19 0.15 0 0
CUI: C0007642
Disease: Cellulitis
Cellulitis 		38 0 14 0.15 0 0
CUI: C0494261
Disease: Combined immunodeficiency
Combined immunodeficiency 		86 0 19 0.14 0 0
CUI: C1855067
Disease: B lymphocytopenia
B lymphocytopenia 		13 0 10 0.14 0 0
CUI: C1854495
Disease: Recurrent infection of the gastrointestinal tract
Recurrent infection of the gastrointestinal tract 		16 0 10 0.13 0 0
CUI: C3665596
Disease: Warts
Warts 		39 0 12 0.12 0 0
CUI: C0037199
Disease: Sinusitis
Sinusitis 		97 0 18 0.12 0 0
CUI: C0694550
Disease: Recurrent pneumonia
Recurrent pneumonia 		62 0 14 0.12 0 0
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood 		75 0 15 0.12 0 0
CUI: C0043037
Disease: Common wart
Common wart 		48 0 12 0.11 0 0
CUI: C2936665
Disease: Immunoglobulin Deficiency, Late-Onset
Immunoglobulin Deficiency, Late-Onset 		11 0 8 0.11 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		95 0 16 0.11 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 15 0.10 0 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		70 0 13 0.10 0 0
CUI: C0398686
Disease: Primary immune deficiency disorder
Primary immune deficiency disorder 		93 0 15 0.10 0 0
CUI: C0741796
Disease: Recurrent bronchitis
Recurrent bronchitis 		29 0 9 0.10 0 0
CUI: C1832241
Disease: Agammaglobulinemia, non-Bruton type
Agammaglobulinemia, non-Bruton type 		8 0 7 1.0E-01 0 0
CUI: C1328587
Disease: Panhypogammaglobulinemia
Panhypogammaglobulinemia 		20 0 8 9.9E-02 0 0
CUI: C0398689
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 1
Hyper-IgM Immunodeficiency Syndrome, Type 1 		33 0 9 9.7E-02 0 0
CUI: C0024312
Disease: Lymphopenia
Lymphopenia 		239 0 27 9.6E-02 0 0
CUI: C1848389
Disease: Posterior pharyngeal cleft
Posterior pharyngeal cleft 		12 0 7 9.5E-02 0 0