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: C0864632
Disease: dmac
dmac
4 0 2 0.17 0 0
Slowly progressive insulin dependent diabetes
4 0 2 0.17 0 0
CUI: C1959859
Disease: Acute lyme disease
Acute lyme disease
4 0 2 0.17 0 0
CUI: C3826217
Disease: Hepatitis in children
Hepatitis in children
4 0 2 0.17 0 0
CUI: C4302167
Disease: Autoimmune myopathy
Autoimmune myopathy
4 0 2 0.17 0 0
CUI: C0023788
Disease: Whipple Disease
Whipple Disease
5 0 2 0.15 0 0
CUI: C0264478
Disease: Sequoiosis
Sequoiosis
5 0 2 0.15 0 0
Diffuse infiltrative lymphocytosis syndrome
5 0 2 0.15 0 0
CUI: C3898352
Disease: Mild Bronchopulmonary Dysplasia
Mild Bronchopulmonary Dysplasia
5 0 2 0.15 0 0
CUI: C0034888
Disease: Rectal Prolapse
Rectal Prolapse
46 0 7 0.14 0 0
CUI: C0577620
Disease: Nut Hypersensitivity
Nut Hypersensitivity
6 0 2 0.14 0 0
CUI: C0854359
Disease: Insulin autoimmune syndrome
Insulin autoimmune syndrome
6 0 2 0.14 0 0
CUI: C1510449
Disease: Chronic iridocyclitis
Chronic iridocyclitis
6 0 2 0.14 0 0
CUI: C1868193
Disease: PNEUMOTHORAX, PRIMARY SPONTANEOUS
PNEUMOTHORAX, PRIMARY SPONTANEOUS
46 0 7 0.14 0 0
CUI: C1956391
Disease: Temporal Arteritis
Temporal Arteritis
6 0 2 0.14 0 0
CUI: C2887821
Disease: Left sided colitis
Left sided colitis
6 0 2 0.14 0 0
CUI: C3888521
Disease: Autoimmune demyelinating disease
Autoimmune demyelinating disease
6 0 2 0.14 0 0
CUI: C1262147
Disease: Scleroderma renal crisis
Scleroderma renal crisis
7 0 2 0.13 0 0
Tubulointerstitial nephritis and uveitis
7 0 2 0.13 0 0
CUI: C3711850
Disease: Opticospinal Multiple Sclerosis
Opticospinal Multiple Sclerosis
7 0 2 0.13 0 0
Myopathy, familial idiopathic inflammatory
7 0 2 0.13 0 0
Primary Progressive Aphasia (disorder)
51 0 7 0.13 0 0
CUI: C0019343
Disease: Pemphigoid Gestationis
Pemphigoid Gestationis
8 0 2 0.12 0 0
Undifferentiated spondyloarthropathy
8 0 2 0.12 0 0
CUI: C0014583
Disease: Episcleritis
Episcleritis
9 0 2 0.12 0 0