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: C4477053
Disease: Decreased proportion of CD3-positive T cells
Decreased proportion of CD3-positive T cells 		9 0 5 7.6E-02 0 0
CUI: C0085110
Disease: Severe Combined Immunodeficiency
Severe Combined Immunodeficiency 		284 0 24 7.5E-02 0 0
CUI: C0033774
Disease: Pruritus
Pruritus 		107 0 11 7.0E-02 0 0
CUI: C1274233
Disease: T-lymphocyte immunodeficiency
T-lymphocyte immunodeficiency 		15 0 5 6.9E-02 0 0
CUI: C0497156
Disease: Lymphadenopathy
Lymphadenopathy 		277 0 22 6.9E-02 0 0
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		127 0 12 6.8E-02 0 0
CUI: C0268124
Disease: Adenosine deaminase deficiency
Adenosine deaminase deficiency 		17 0 5 6.8E-02 0 0
CUI: C0024312
Disease: Lymphopenia
Lymphopenia 		239 0 19 6.7E-02 0 0
CUI: C0002880
Disease: Autoimmune hemolytic anemia
Autoimmune hemolytic anemia 		81 0 9 6.7E-02 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis 		97 0 10 6.7E-02 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 6 6.7E-02 0 0
CUI: C0581381
Disease: Recurrent upper respiratory tract infection
Recurrent upper respiratory tract infection 		52 0 7 6.5E-02 0 0
CUI: C0005741
Disease: Blepharitis
Blepharitis 		55 0 7 6.4E-02 0 0
CUI: C0700216
Disease: Structural Clinical Interview for DSM-III
Structural Clinical Interview for DSM-III 		5 0 4 6.3E-02 0 0
CUI: C1849236
Disease: Severe combined immunodeficiency, atypical
Severe combined immunodeficiency, atypical 		5 0 4 6.3E-02 0 0
CUI: C0013604
Disease: Edema
Edema 		126 0 11 6.2E-02 0 0
CUI: C0392607
Disease: Severe combined immunodeficiency due to adenosine deaminase deficiency
Severe combined immunodeficiency due to adenosine deaminase deficiency 		24 0 5 6.2E-02 0 0
CUI: C1744558
Disease: T-lymphocyte deficiency
T-lymphocyte deficiency 		25 0 5 6.1E-02 0 0
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		95 0 9 6.1E-02 0 0
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		166 122 13 6.0E-02 3 2.3E-02
CUI: C1842777
Disease: Recurrent upper and lower respiratory tract infections
Recurrent upper and lower respiratory tract infections 		10 0 4 5.9E-02 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 13 5.8E-02 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 13 5.8E-02 0 0
CUI: C0578878
Disease: Inflammation of large intestine
Inflammation of large intestine 		12 0 4 5.7E-02 0 0
CUI: C1860128
Disease: Recurrent candida infections
Recurrent candida infections 		12 0 4 5.7E-02 0 0