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: C0276876
Disease: Infection by Leishmania infantum
Infection by Leishmania infantum
1 0 1 0.20 0 0
CUI: C0391860
Disease: Diffuse inflammation
Diffuse inflammation
1 0 1 0.20 0 0
CUI: C0518959
Disease: Left atrial myxoma
Left atrial myxoma
1 0 1 0.20 0 0
MALARIA, CEREBRAL, SUSCEPTIBILITY TO (finding)
1 0 1 0.20 0 0
CUI: C2350449
Disease: Pancreatitis, Graft
Pancreatitis, Graft
1 0 1 0.20 0 0
CUI: C2919576
Disease: Left sided ulcerative colitis
Left sided ulcerative colitis
1 0 1 0.20 0 0
CUI: C4706275
Disease: Sickle cell hepatopathy
Sickle cell hepatopathy
1 0 1 0.20 0 0
CUI: C0014736
Disease: Erysipelothrix infection
Erysipelothrix infection
2 0 1 0.17 0 0
CUI: C0025427
Disease: Mercury Poisoning
Mercury Poisoning
3 0 1 0.14 0 0
CUI: C0025472
Disease: Mesenteric Vascular Occlusion
Mesenteric Vascular Occlusion
3 0 1 0.14 0 0
CUI: C0266913
Disease: Hyperplastic gingivitis
Hyperplastic gingivitis
3 0 1 0.14 0 0
CUI: C1841651
Disease: Heme Oxygenase 1 Deficiency
Heme Oxygenase 1 Deficiency
3 0 1 0.14 0 0
CUI: C2937222
Disease: Chronic ulcerative proctitis
Chronic ulcerative proctitis
3 0 1 0.14 0 0
CUI: C0007020
Disease: Carbon Monoxide Poisoning
Carbon Monoxide Poisoning
4 0 1 0.12 0 0
CUI: C0263222
Disease: Chronic eczema
Chronic eczema
4 0 1 0.12 0 0
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
4 0 1 0.12 0 0
CUI: C2609079
Disease: Mirror syndrome
Mirror syndrome
4 0 1 0.12 0 0
Malignant neoplasm of upper third of esophagus
5 0 1 0.11 0 0
Malignant neoplasm of middle third of esophagus
5 0 1 0.11 0 0
Malignant neoplasm of lower third of esophagus
5 0 1 0.11 0 0
Malignant neoplasm of other specified part of esophagus
5 0 1 0.11 0 0
CUI: C0391820
Disease: Gouty nephropathy
Gouty nephropathy
5 0 1 0.11 0 0
Malignant neoplasm of abdominal part of esophagus
5 0 1 0.11 0 0
CUI: C0497249
Disease: hypertension complicated
hypertension complicated
5 0 1 0.11 0 0
CUI: C0948031
Disease: Primary Graft Dysfunction
Primary Graft Dysfunction
5 0 1 0.11 0 0