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: C1144799
Disease: Hypertensive cardiomyopathy
Hypertensive cardiomyopathy
3 0 2 0.25 0 0
CUI: C0268707
Disease: Uremic encephalopathy
Uremic encephalopathy
5 0 2 0.20 0 0
CUI: C1274999
Disease: Skin flap necrosis
Skin flap necrosis
5 0 2 0.20 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia
7 0 2 0.17 0 0
Dissecting Abdominal Aortic Aneurysm
7 0 2 0.17 0 0
CUI: C0406500
Disease: Lipodermatosclerosis
Lipodermatosclerosis
14 0 3 0.17 0 0
cutaneous B-cell non-Hodgkin lymphoma
16 0 3 0.15 0 0
CUI: C0032044
Disease: Placenta Accreta
Placenta Accreta
1 0 1 0.14 0 0
CUI: C0268889
Disease: Prostatic Obstruction
Prostatic Obstruction
1 0 1 0.14 0 0
Curly hair-ankyloblepharon-nail dysplasia syndrome
1 0 1 0.14 0 0
CUI: C0600039
Disease: Urinary outflow obstruction
Urinary outflow obstruction
1 0 1 0.14 0 0
Recurrent Childhood Hepatocellular Carcinoma
1 0 1 0.14 0 0
Recurrent Adult Hepatocellular Carcinoma
1 0 1 0.14 0 0
VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL
1 0 1 0.14 0 0
CUI: C2853945
Disease: Non-follicular lymphoma
Non-follicular lymphoma
1 0 1 0.14 0 0
CUI: C3160915
Disease: Corneal thickening
Corneal thickening
1 0 1 0.14 0 0
CUI: C4021877
Disease: Agenesis of maxillary incisor
Agenesis of maxillary incisor
1 0 1 0.14 0 0
CUI: C4310639
Disease: GLAUCOMA 3, PRIMARY CONGENITAL, E
GLAUCOMA 3, PRIMARY CONGENITAL, E
1 0 1 0.14 0 0
Acute myeloid leukemia with CEBPA somatic mutations
1 0 1 0.14 0 0
Metastatic Bladder Urothelial Carcinoma
1 0 1 0.14 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity
2 0 1 0.12 0 0
CUI: C0153562
Disease: Kaposi's sarcoma of palate
Kaposi's sarcoma of palate
2 0 1 0.12 0 0
Renal Pelvis and Ureter Urothelial Carcinoma
2 0 1 0.12 0 0
Velamentous insertion of umbilical cord (disorder)
2 0 1 0.12 0 0
CUI: C0343208
Disease: Essential mixed cryoglobulinemia
Essential mixed cryoglobulinemia
2 0 1 0.12 0 0