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: C4748863
Disease: LYMPHOPROLIFERATIVE SYNDROME 3
LYMPHOPROLIFERATIVE SYNDROME 3 		2 0 1 0.50 0 0
CUI: C3554540
Disease: LYMPHOPROLIFERATIVE SYNDROME 2
LYMPHOPROLIFERATIVE SYNDROME 2 		3 0 1 0.33 0 0
CUI: C1701919
Disease: EBV viremia
EBV viremia 		7 0 1 0.14 0 0
CUI: C4749304
Disease: Monosomy 13q14 syndrome
Monosomy 13q14 syndrome 		7 0 1 0.14 0 0
CUI: C0026976
Disease: Myelitis, Transverse
Myelitis, Transverse 		8 0 1 0.12 0 0
CUI: C1847973
Disease: Persistent Polyclonal B-Cell Lymphocytosis
Persistent Polyclonal B-Cell Lymphocytosis 		8 0 1 0.12 0 0
CUI: C3275445
Disease: X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia 		11 0 1 9.1E-02 0 0
CUI: C0409652
Disease: Seronegative rheumatoid arthritis
Seronegative rheumatoid arthritis 		12 0 1 8.3E-02 0 0
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		22 0 1 4.5E-02 0 0
CUI: C0398689
Disease: Hyper-IgM Immunodeficiency Syndrome, Type 1
Hyper-IgM Immunodeficiency Syndrome, Type 1 		33 0 1 3.0E-02 0 0
CUI: C0024140
Disease: Lupus Erythematosus, Subacute Cutaneous
Lupus Erythematosus, Subacute Cutaneous 		39 0 1 2.6E-02 0 0
CUI: C0549463
Disease: X-Linked Lymphoproliferative Disorder
X-Linked Lymphoproliferative Disorder 		49 0 1 2.0E-02 0 0
CUI: C1704423
Disease: Milroy Disease
Milroy Disease 		52 0 1 1.9E-02 0 0
CUI: C2921627
Disease: Clinically isolated syndrome
Clinically isolated syndrome 		54 0 1 1.9E-02 0 0
CUI: C4025886
Disease: Severe periodontitis
Severe periodontitis 		54 0 1 1.9E-02 0 0
CUI: C0543697
Disease: Mixed cryoglobulinemia
Mixed cryoglobulinemia 		56 0 1 1.8E-02 0 0
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
Tuberculosis, extrapulmonary 		58 0 1 1.7E-02 0 0
CUI: C4524268
Disease: Advanced lung cancer
Advanced lung cancer 		59 0 1 1.7E-02 0 0
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		61 0 1 1.6E-02 0 0
CUI: C1328840
Disease: Autoimmune Lymphoproliferative Syndrome
Autoimmune Lymphoproliferative Syndrome 		65 0 1 1.5E-02 0 0
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood 		75 0 1 1.3E-02 0 0
CUI: C0086438
Disease: Hypogammaglobulinemia
Hypogammaglobulinemia 		76 0 1 1.3E-02 0 0
CUI: C0432408
Disease: Trisomy 12
Trisomy 12 		76 0 1 1.3E-02 0 0
CUI: C0024282
Disease: Lymphocytosis
Lymphocytosis 		78 0 1 1.3E-02 0 0
CUI: C0029134
Disease: Optic Neuritis
Optic Neuritis 		79 0 1 1.3E-02 0 0