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: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate
10 0 5 0.12 0 0
CUI: C0521618
Disease: Stenosis of ureter
Stenosis of ureter
10 0 5 0.12 0 0
CUI: C0005138
Disease: Berylliosis
Berylliosis
11 0 5 0.12 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia
248 0 30 0.12 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3
12 0 5 0.12 0 0
CUI: C2350873
Disease: Beryllium Disease
Beryllium Disease
12 0 5 0.12 0 0
CUI: C3887590
Disease: Stricture of ureter
Stricture of ureter
12 0 5 0.12 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 5 0.12 0 0
CUI: C0032231
Disease: Pleurisy
Pleurisy
82 0 12 0.11 0 0
CUI: C0521173
Disease: Granulomatosis
Granulomatosis
14 0 5 0.11 0 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity
15 0 5 0.11 0 0
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
26 0 6 0.11 0 0
Hereditary Autoinflammatory Diseases
16 0 5 0.11 0 0
CUI: C0035021
Disease: Relapsing Fever
Relapsing Fever
48 0 8 0.11 0 0
CUI: C0585274
Disease: Periodic syndrome
Periodic syndrome
6 0 4 0.11 0 0
CUI: C3714772
Disease: Recurrent fevers
Recurrent fevers
48 0 8 0.11 0 0
Cryopyrin-Associated Periodic Syndromes
39 0 7 0.10 0 0
CUI: C0015974
Disease: Periodic fever
Periodic fever
19 0 5 1.0E-01 0 0
CUI: C0034735
Disease: Raynaud Phenomenon
Raynaud Phenomenon
63 0 9 1.0E-01 0 0
CUI: C1519353
Disease: Skin Papule
Skin Papule
74 0 10 1.0E-01 0 0
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis
53 0 8 9.9E-02 0 0
CUI: C0332563
Disease: Papule
Papule
76 0 10 9.8E-02 0 0
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase
20 0 5 9.8E-02 0 0
Systemic onset juvenile chronic arthritis
90 0 11 9.6E-02 0 0
CUI: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies
81 0 10 9.3E-02 0 0