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: C0022073
Disease: Iridocyclitis
Iridocyclitis 		16 0 9 0.23 0 0
CUI: C4023452
Disease: Elevated C-reactive protein level
Elevated C-reactive protein level 		28 0 11 0.22 0 0
CUI: C0151632
Disease: ESR raised
ESR raised 		36 0 11 0.19 0 0
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		30 0 8 0.15 0 0
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		26 0 7 0.13 0 0
CUI: C0031046
Disease: Pericarditis
Pericarditis 		51 0 9 0.12 0 0
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive 		35 0 7 0.11 0 0
CUI: C1857108
Disease: Limitation of joint mobility
Limitation of joint mobility 		84 0 12 0.11 0 0
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		26 0 6 0.11 0 0
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		51 0 8 0.11 0 0
CUI: C0162323
Disease: Polyarthritis
Polyarthritis 		65 0 9 0.10 0 0
CUI: C0005138
Disease: Berylliosis
Berylliosis 		11 0 4 1.0E-01 0 0
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		90 0 11 9.8E-02 0 0
CUI: C2350873
Disease: Beryllium Disease
Beryllium Disease 		12 0 4 9.8E-02 0 0
CUI: C4023588
Disease: Abnormality of the gastrointestinal tract
Abnormality of the gastrointestinal tract 		14 0 4 9.3E-02 0 0
CUI: C4025038
Disease: Abnormality of the tibial metaphysis
Abnormality of the tibial metaphysis 		3 0 3 9.1E-02 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia 		248 0 23 8.9E-02 0 0
CUI: C4025040
Disease: Abnormality of the femoral metaphysis
Abnormality of the femoral metaphysis 		4 0 3 8.8E-02 0 0
CUI: C0272350
Disease: Dysfibrinogenemia, Congenital
Dysfibrinogenemia, Congenital 		6 0 3 8.3E-02 0 0
CUI: C2584774
Disease: Congenital hypofibrinogenemia
Congenital hypofibrinogenemia 		6 0 3 8.3E-02 0 0
CUI: C3463916
Disease: Complement Factor I (C3 inactivator) deficiency
Complement Factor I (C3 inactivator) deficiency 		6 0 3 8.3E-02 0 0
CUI: C0235986
Disease: Growth hormone excess
Growth hormone excess 		20 0 4 8.2E-02 0 0
CUI: C0267561
Disease: Perianal fistula
Perianal fistula 		7 0 3 8.1E-02 0 0
CUI: C4721411
Disease: Osteolysis
Osteolysis 		62 0 7 8.0E-02 0 0
CUI: C0016663
Disease: Pathological fracture
Pathological fracture 		35 0 5 7.9E-02 0 0