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: C1096527
Disease: Mosaic trisomy 8 syndrome
Mosaic trisomy 8 syndrome
4 0 3 0.50 0 0
CUI: C3666010
Disease: Breakthrough infection
Breakthrough infection
2 0 2 0.40 0 0
CUI: C4510988
Disease: Monogenic autoinflammatory syndrome
Monogenic autoinflammatory syndrome
2 0 2 0.40 0 0
CUI: C0795940
Disease: Filippi syndrome
Filippi syndrome
6 0 3 0.38 0 0
CUI: C0282312
Disease: Bubonic Plague
Bubonic Plague
3 0 2 0.33 0 0
CUI: C0392777
Disease: Poikiloderma
Poikiloderma
7 0 3 0.33 0 0
Peroxisomal ACYL-COA oxidase deficiency
3 0 2 0.33 0 0
CUI: C1850568
Disease: Nakajo syndrome
Nakajo syndrome
3 0 2 0.33 0 0
Scleritis and episcleritis (disorder)
3 0 2 0.33 0 0
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
3 0 2 0.33 0 0
CUI: C4707790
Disease: Idiopathic recurrent pericarditis
Idiopathic recurrent pericarditis
3 0 2 0.33 0 0
PLCG2-associated antibody deficiency and immune dysregulation
3 0 2 0.33 0 0
CUI: C0034734
Disease: Raynaud Disease
Raynaud Disease
4 0 2 0.29 0 0
CUI: C0206114
Disease: Periodontal Attachment Loss
Periodontal Attachment Loss
4 0 2 0.29 0 0
CUI: C0277561
Disease: Juvenile disease
Juvenile disease
4 0 2 0.29 0 0
Still's disease with juvenile onset and/or adult onset
4 0 2 0.29 0 0
CUI: C4076304
Disease: Dental plaque induced gingivitis
Dental plaque induced gingivitis
4 0 2 0.29 0 0
CUI: C0006664
Disease: Calcinosis cutis
Calcinosis cutis
5 0 2 0.25 0 0
CUI: C0403528
Disease: Henoch-Schönlein nephritis
Henoch-Schönlein nephritis
5 0 2 0.25 0 0
CUI: C1304193
Disease: Chronic autoimmune urticaria
Chronic autoimmune urticaria
5 0 2 0.25 0 0
Nonrheumatic aortic (valve) stenosis
5 0 2 0.25 0 0
CUI: C0265372
Disease: Fetal hydantoin syndrome
Fetal hydantoin syndrome
11 0 3 0.23 0 0
CUI: C0919907
Disease: Pleural Infection
Pleural Infection
6 0 2 0.22 0 0
Parenteral nutrition associated liver disease
6 0 2 0.22 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing
1 0 1 0.20 0 0