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: C1842528
Disease: Impaired Ig class switch recombination
Impaired Ig class switch recombination 		4 0 4 0.33 0 0
CUI: C0398689
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 1
Hyper-IgM Immunodeficiency Syndrome, Type 1 		33 22 10 0.29 1 4.5E-02
CUI: C1720956
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 2
Hyper-IgM Immunodeficiency Syndrome, Type 2 		3 0 3 0.25 0 0
CUI: C1720957
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 3
Hyper-IgM Immunodeficiency Syndrome, Type 3 		3 0 3 0.25 0 0
CUI: C1720958
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 5
Hyper-IgM Immunodeficiency Syndrome, Type 5 		3 0 3 0.25 0 0
CUI: C1863767
Disease: Light Fixation Seizure Syndrome
Light Fixation Seizure Syndrome 		3 0 3 0.25 0 0
CUI: C4025672
Disease: Impaired memory B cell generation
Impaired memory B cell generation 		3 0 3 0.25 0 0
CUI: C0035921
Disease: Congenital Rubella Syndrome
Congenital Rubella Syndrome 		3 0 2 0.15 0 0
CUI: C0221065
Disease: Subacute Combined Degeneration
Subacute Combined Degeneration 		3 0 2 0.15 0 0
CUI: C1846008
Disease: HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC
HYPER-IgM IMMUNODEFICIENCY, X-LINKED, WITH ECTODERMAL DYSPLASIA, HYPOHIDROTIC 		3 0 2 0.15 0 0
CUI: C1847383
Disease: Absence of lymph node germinal center
Absence of lymph node germinal center 		4 0 2 0.14 0 0
CUI: C1704378
Disease: Heymann Nephritis
Heymann Nephritis 		13 0 3 0.14 0 0
CUI: C3472600
Disease: Chronic hepatitis E
Chronic hepatitis E 		5 0 2 0.13 0 0
CUI: C1608955
Disease: Mycobacterium abscessus Infection
Mycobacterium abscessus Infection 		6 0 2 0.12 0 0
CUI: C4049279
Disease: Post stroke epilepsy
Post stroke epilepsy 		7 0 2 0.12 0 0
CUI: C0745242
Disease: Immunoglobulin deficiency
Immunoglobulin deficiency 		8 0 2 0.11 0 0
CUI: C1279481
Disease: X-Linked Combined Immunodeficiency Diseases
X-Linked Combined Immunodeficiency Diseases 		38 0 5 0.11 0 0
CUI: C1847973
Disease: Persistent Polyclonal B-Cell Lymphocytosis
Persistent Polyclonal B-Cell Lymphocytosis 		8 0 2 0.11 0 0
CUI: C0013374
Disease: Dysgammaglobulinemia
Dysgammaglobulinemia 		10 0 2 1.0E-01 0 0
CUI: C1842777
Disease: Recurrent upper and lower respiratory tract infections
Recurrent upper and lower respiratory tract infections 		10 0 2 1.0E-01 0 0
CUI: C1846006
Disease: Ectodermal dysplasia, hypohidrotic, with immune deficiency
Ectodermal dysplasia, hypohidrotic, with immune deficiency 		10 0 2 1.0E-01 0 0
CUI: C0878552
Disease: Coronary artery ectasia
Coronary artery ectasia 		24 0 3 9.1E-02 0 0
CUI: C0948343
Disease: Transfusion-Related Acute Lung Injury
Transfusion-Related Acute Lung Injury 		24 0 3 9.1E-02 0 0
CUI: C0476486
Disease: Generalized enlarged lymph nodes
Generalized enlarged lymph nodes 		13 0 2 8.7E-02 0 0
CUI: C4749333
Disease: Refractory celiac disease
Refractory celiac disease 		13 0 2 8.7E-02 0 0