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: C0149910
Disease: Intermittent joint effusion
Intermittent joint effusion
2 0 2 0.22 0 0
Inflammatory myopathy with abundant macrophages
2 0 2 0.22 0 0
Encephalitis caused by tick-borne encephalitis virus
5 0 2 0.17 0 0
CUI: C0024205
Disease: Lymphadenitis
Lymphadenitis
55 2 9 0.16 1 0.50
CUI: C0585274
Disease: Periodic syndrome
Periodic syndrome
6 0 2 0.15 0 0
Tumor necrosis factor receptor associated periodic syndrome [TRAPS]
6 2 2 0.15 1 0.50
CUI: C0860236
Disease: Disseminated leishmaniasis
Disseminated leishmaniasis
8 0 2 0.13 0 0
CUI: C0742960
Disease: cyst benign
cyst benign
9 0 2 0.12 0 0
CUI: C0015974
Disease: Periodic fever
Periodic fever
19 5 3 0.12 1 0.20
CUI: C0024759
Disease: Mansonelliasis
Mansonelliasis
10 0 2 0.12 0 0
CUI: C0948853
Disease: Euthymia
Euthymia
10 0 2 0.12 0 0
CUI: C0026471
Disease: Monoclonal paraproteinemia
Monoclonal paraproteinemia
1 0 1 0.11 0 0
CUI: C0858613
Disease: Optic nerve oedema
Optic nerve oedema
1 0 1 0.11 0 0
Lower respiratory tract inflammation
1 0 1 0.11 0 0
CUI: C1262216
Disease: IgM gammopathy
IgM gammopathy
1 0 1 0.11 0 0
CUI: C1389289
Disease: BB leprosy
BB leprosy
1 0 1 0.11 0 0
MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1
1 0 1 0.11 0 0
Familial Mediterranean Fever, Autosomal Dominant
1 0 1 0.11 0 0
CUI: C2350879
Disease: Tropical Eosinophilic Pneumonia
Tropical Eosinophilic Pneumonia
1 0 1 0.11 0 0
CUI: C2677101
Disease: Inflammatory Bowel Disease 13
Inflammatory Bowel Disease 13
1 0 1 0.11 0 0
Familial Waldenstrom's Macroglobulinaemia
1 0 1 0.11 0 0
CUI: C4054892
Disease: Grade II Chondrosarcoma
Grade II Chondrosarcoma
1 0 1 0.11 0 0
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS
1 0 1 0.11 0 0
Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome [PFAPA]
1 0 1 0.11 0 0
Monoclonal immunoglobulin M proteinemia
1 0 1 0.11 0 0