Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Zoonotic form of cutaneous leishmaniasis
6 0 2 9.1E-02 0 0
CUI: C2887821
Disease: Left sided colitis
Left sided colitis
6 0 2 9.1E-02 0 0
CUI: C3826476
Disease: Dental caries in children
Dental caries in children
6 0 2 9.1E-02 0 0
CUI: C3872662
Disease: Chronic active hepatitis C
Chronic active hepatitis C
18 0 3 9.1E-02 0 0
CUI: C0030804
Disease: Pemphigoid, Benign Mucous Membrane
Pemphigoid, Benign Mucous Membrane
19 0 3 8.8E-02 0 0
CUI: C0751057
Disease: Seizure, Febrile, Complex
Seizure, Febrile, Complex
19 0 3 8.8E-02 0 0
CUI: C0267561
Disease: Perianal fistula
Perianal fistula
7 0 2 8.7E-02 0 0
CUI: C1096116
Disease: Acquired haemophilia
Acquired haemophilia
7 0 2 8.7E-02 0 0
Tubulointerstitial nephritis and uveitis
7 0 2 8.7E-02 0 0
CUI: C0024228
Disease: Lymphatic Diseases
Lymphatic Diseases
8 0 2 8.3E-02 0 0
CUI: C0026265
Disease: Diseases of mitral valve
Diseases of mitral valve
21 0 3 8.3E-02 0 0
Hantavirus infection in conditions classified elsewhere and of unspecified site
21 0 3 8.3E-02 0 0
CUI: C0399447
Disease: Early onset periodontitis
Early onset periodontitis
21 0 3 8.3E-02 0 0
CUI: C0744471
Disease: Gram-negative bacteremia
Gram-negative bacteremia
8 0 2 8.3E-02 0 0
CUI: C1262113
Disease: Lipohypertrophy
Lipohypertrophy
8 0 2 8.3E-02 0 0
Undifferentiated spondyloarthropathy
8 0 2 8.3E-02 0 0
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
22 0 3 8.1E-02 0 0
CUI: C0085253
Disease: Adult-Onset Still Disease
Adult-Onset Still Disease
76 0 7 8.0E-02 0 0
CUI: C0031022
Disease: Chronic periaortitis
Chronic periaortitis
9 0 2 8.0E-02 0 0
CUI: C0149517
Disease: Chronic tonsillitis
Chronic tonsillitis
9 0 2 8.0E-02 0 0
CUI: C0240903
Disease: Rheumatoid Vasculitis
Rheumatoid Vasculitis
9 0 2 8.0E-02 0 0
CUI: C0242993
Disease: Nephropathia Epidemica
Nephropathia Epidemica
9 0 2 8.0E-02 0 0
CUI: C1527396
Disease: Fibrocystic Disease of Pancreas
Fibrocystic Disease of Pancreas
9 0 2 8.0E-02 0 0
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome
23 0 3 7.9E-02 0 0
Severe hereditary factor VIII deficiency disease
37 0 4 7.8E-02 0 0