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: C0041315
Disease: Tuberculosis, Laryngeal
Tuberculosis, Laryngeal
1 0 1 6.7E-03 0 0
CUI: C0042171
Disease: Uveoparotid Fever
Uveoparotid Fever
1 0 1 6.7E-03 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma
1 0 1 6.7E-03 0 0
CUI: C0085668
Disease: Secondary carcinoma
Secondary carcinoma
1 0 1 6.7E-03 0 0
CUI: C0085740
Disease: Mendelson Syndrome
Mendelson Syndrome
1 0 1 6.7E-03 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis
1 0 1 6.7E-03 0 0
CUI: C0151536
Disease: Stenosis of bronchus
Stenosis of bronchus
1 0 1 6.7E-03 0 0
CUI: C0152089
Disease: Post-laminectomy syndrome
Post-laminectomy syndrome
1 0 1 6.7E-03 0 0
Food poisoning caused by Vibrio parahaemolyticus
1 0 1 6.7E-03 0 0
CUI: C0152902
Disease: Tuberculosis of esophagus
Tuberculosis of esophagus
1 0 1 6.7E-03 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication
1 0 1 6.7E-03 0 0
CUI: C0153661
Disease: Malignant neoplasm of thorax
Malignant neoplasm of thorax
1 0 1 6.7E-03 0 0
CUI: C0154064
Disease: Carcinoma in situ of anus
Carcinoma in situ of anus
1 0 1 6.7E-03 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea
1 0 1 6.7E-03 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation
1 0 1 6.7E-03 0 0
CUI: C0232910
Disease: Teratogenesis
Teratogenesis
1 0 1 6.7E-03 0 0
CUI: C0233599
Disease: Bar-biting
Bar-biting
1 0 1 6.7E-03 0 0
CUI: C0234959
Disease: Panarteritis
Panarteritis
1 0 1 6.7E-03 0 0
CUI: C0235267
Disease: Redness of eye
Redness of eye
1 0 1 6.7E-03 0 0
CUI: C0235453
Disease: Steroid withdrawal syndrome
Steroid withdrawal syndrome
1 0 1 6.7E-03 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia
1 0 1 6.7E-03 0 0
CUI: C0235876
Disease: Depression aggravated
Depression aggravated
1 0 1 6.7E-03 0 0
CUI: C0235952
Disease: Clostridium difficile diarrhea
Clostridium difficile diarrhea
1 0 1 6.7E-03 0 0
Disorder of male reproductive system
1 0 1 6.7E-03 0 0
CUI: C0238120
Disease: Acquired Factor XIII Deficiency
Acquired Factor XIII Deficiency
1 0 1 6.7E-03 0 0