Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Immunoglobulin A deficiency (disorder)
72 25 28 0.31 19 0.66
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus
51 0 13 0.16 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
89 0 18 0.16 0 0
CUI: C4087124
Disease: Immunoglobulin G4-Related Disease
Immunoglobulin G4-Related Disease
80 0 15 0.14 0 0
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
207 0 29 0.13 0 0
CUI: C0037023
Disease: Sialadenitis
Sialadenitis
42 0 10 0.13 0 0
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
43 0 10 0.13 0 0
CUI: C3495436
Disease: American cutaneous leishmaniasis
American cutaneous leishmaniasis
19 0 7 0.12 0 0
CUI: C0030807
Disease: Pemphigus
Pemphigus
67 0 12 0.12 0 0
CUI: C0409651
Disease: Seropositive rheumatoid arthritis
Seropositive rheumatoid arthritis
30 0 8 0.12 0 0
CUI: C0015773
Disease: Felty Syndrome
Felty Syndrome
13 0 6 0.12 0 0
CUI: C1304140
Disease: Familial psoriasis
Familial psoriasis
13 0 6 0.12 0 0
CUI: C0041316
Disease: Lymph Node Tuberculosis
Lymph Node Tuberculosis
33 0 8 0.11 0 0
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome
102 0 15 0.11 0 0
CUI: C0042167
Disease: Uveitis, Posterior
Uveitis, Posterior
24 0 7 0.11 0 0
CUI: C0948201
Disease: Alloimmunisation
Alloimmunisation
65 0 11 0.11 0 0
CUI: C0021345
Disease: Infectious Mononucleosis
Infectious Mononucleosis
58 0 10 0.11 0 0
Tubulointerstitial nephritis and uveitis
7 0 5 0.11 0 0
CUI: C0522274
Disease: Humoral immune defect
Humoral immune defect
29 0 7 0.10 0 0
CUI: C0868908
Disease: Pancolitis
Pancolitis
29 0 7 0.10 0 0
CUI: C0271073
Disease: Eales disease
Eales disease
9 0 5 0.10 0 0
CUI: C1304469
Disease: Localized vitiligo
Localized vitiligo
9 0 5 0.10 0 0
CUI: C0151450
Disease: Secondary Sjögren's syndrome
Secondary Sjögren's syndrome
20 0 6 0.10 0 0
Aspergillosis, Allergic Bronchopulmonary
31 0 7 0.10 0 0
Chromosome 11p11.2 Deletion Syndrome
65 0 10 1.0E-01 0 0