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: C2363819
Disease: Paucigranulocytic asthma
Paucigranulocytic asthma
10 0 8 0.19 0 0
CUI: C0340076
Disease: Asthmatic pulmonary eosinophilia
Asthmatic pulmonary eosinophilia
62 0 16 0.19 0 0
CUI: C0034068
Disease: Pulmonary Eosinophilia
Pulmonary Eosinophilia
70 0 16 0.17 0 0
CUI: C0684256
Disease: Bacterial sepsis
Bacterial sepsis
38 0 11 0.16 0 0
Hereditary Autoinflammatory Diseases
16 0 7 0.14 0 0
CUI: C2955673
Disease: Urate nephropathy
Urate nephropathy
16 0 7 0.14 0 0
CUI: C1850383
Disease: Neuropathy, Painful
Neuropathy, Painful
18 0 7 0.14 0 0
CUI: C0343068
Disease: Familial cold urticaria
Familial cold urticaria
20 0 7 0.13 0 0
Cryopyrin-Associated Periodic Syndromes
39 0 9 0.13 0 0
CUI: C0267375
Disease: Chronic colitis
Chronic colitis
57 0 11 0.13 0 0
CUI: C0343466
Disease: Type 2 lepra reaction
Type 2 lepra reaction
23 0 7 0.12 0 0
CUI: C0343467
Disease: Erythema nodosum leprosum
Erythema nodosum leprosum
23 0 7 0.12 0 0
CUI: C4049273
Disease: Systemic immune activation
Systemic immune activation
23 0 7 0.12 0 0
CUI: C0343055
Disease: Generalized pustular psoriasis
Generalized pustular psoriasis
43 0 9 0.12 0 0
CUI: C3890737
Disease: Autoinflammatory Syndrome
Autoinflammatory Syndrome
25 0 7 0.12 0 0
CUI: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome
17 0 6 0.12 0 0
CUI: C1536168
Disease: Chronic pelvic pain syndrome
Chronic pelvic pain syndrome
8 0 5 0.12 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 0 8 0.11 0 0
CUI: C0863129
Disease: AGEP
AGEP
9 0 5 0.11 0 0
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
Henoch-Schonlein purpura nephritis
29 0 7 0.11 0 0
CUI: C0013370
Disease: Amebic colitis
Amebic colitis
49 0 9 0.11 0 0
CUI: C1318973
Disease: Staphylococcus aureus infection
Staphylococcus aureus infection
49 0 9 0.11 0 0
CUI: C0014356
Disease: Enterocolitis
Enterocolitis
40 0 8 0.11 0 0
CUI: C0149896
Disease: Primary gout
Primary gout
40 0 8 0.11 0 0
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase
20 0 6 0.11 0 0