Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Antiphospholipid antibody positivity
18 0 8 0.16 0 0
CUI: C0151632
Disease: ESR raised
ESR raised
36 0 10 0.15 0 0
CUI: C0277942
Disease: Butterfly rash
Butterfly rash
13 0 7 0.15 0 0
CUI: C0338484
Disease: Familial Hemiplegic Migraine
Familial Hemiplegic Migraine
24 0 8 0.14 0 0
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood
8 4 6 0.14 1 0.11
CUI: C0018989
Disease: Hemiparesis
Hemiparesis
91 0 15 0.13 0 0
CUI: C0521173
Disease: Granulomatosis
Granulomatosis
14 0 6 0.12 0 0
CUI: C0278110
Disease: Hemiplegia, Crossed
Hemiplegia, Crossed
5 2 5 0.12 1 0.14
CUI: C1142517
Disease: Lupus anticoagulant measurement
Lupus anticoagulant measurement
5 0 5 0.12 0 0
CUI: C4073169
Disease: Decreased serum complement C4
Decreased serum complement C4
5 0 5 0.12 0 0
CUI: C4321325
Disease: Lupus anticoagulant -- finding
Lupus anticoagulant -- finding
5 0 5 0.12 0 0
CUI: C0426396
Disease: Urine looks dark
Urine looks dark
6 0 5 0.12 0 0
CUI: C3805919
Disease: Recurrent intrapulmonary hemorrhage
Recurrent intrapulmonary hemorrhage
7 0 5 0.12 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine
10 0 5 0.11 0 0
CUI: C0521618
Disease: Stenosis of ureter
Stenosis of ureter
10 0 5 0.11 0 0
CUI: C1837512
Disease: Decreased serum complement C3
Decreased serum complement C3
12 0 5 0.10 0 0
CUI: C3887590
Disease: Stricture of ureter
Stricture of ureter
12 0 5 0.10 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 5 0.10 0 0
CUI: C0151480
Disease: Anti-nuclear factor positive
Anti-nuclear factor positive
35 0 7 0.10 0 0
Abnormality of the gastrointestinal tract
14 0 5 1.0E-01 0 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity
15 0 5 9.8E-02 0 0
CUI: C4023452
Disease: Elevated C-reactive protein level
Elevated C-reactive protein level
28 0 6 9.5E-02 0 0
CUI: C0034735
Disease: Raynaud Phenomenon
Raynaud Phenomenon
63 0 9 9.5E-02 0 0
CUI: C0151857
Disease: Pleocytosis
Pleocytosis
31 0 6 9.1E-02 0 0
CUI: C0221021
Disease: Microangiopathic hemolytic anemia
Microangiopathic hemolytic anemia
31 0 6 9.1E-02 0 0