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: C0002897
Disease: Anemia, Splenic
Anemia, Splenic
1 0 1 9.0E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 9.0E-03 0 0
CUI: C0005723
Disease: Oral paracoccidioidomycosis
Oral paracoccidioidomycosis
1 0 1 9.0E-03 0 0
CUI: C0006264
Disease: Bronchial Neoplasms
Bronchial Neoplasms
1 0 1 9.0E-03 0 0
CUI: C0011871
Disease: Diabetic peripheral angiopathy
Diabetic peripheral angiopathy
1 0 1 9.0E-03 0 0
CUI: C0013426
Disease: Dystrophy of vulva
Dystrophy of vulva
1 0 1 9.0E-03 0 0
CUI: C0017128
Disease: Gastric Fistula
Gastric Fistula
1 0 1 9.0E-03 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male
1 0 1 9.0E-03 0 0
CUI: C0018193
Disease: Granuloma, Foreign-Body
Granuloma, Foreign-Body
1 0 1 9.0E-03 0 0
CUI: C0023869
Disease: Lithiasis
Lithiasis
1 0 1 9.0E-03 0 0
CUI: C0029897
Disease: Otorhinolaryngologic Neoplasms
Otorhinolaryngologic Neoplasms
1 0 1 9.0E-03 0 0
CUI: C0033579
Disease: Prostate nodule
Prostate nodule
1 0 1 9.0E-03 0 0
CUI: C0034882
Disease: Rectal Diseases
Rectal Diseases
1 0 1 9.0E-03 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block
1 0 1 9.0E-03 0 0
CUI: C0040422
Disease: Tonsillar Neoplasms
Tonsillar Neoplasms
1 0 1 9.0E-03 0 0
CUI: C0085668
Disease: Secondary carcinoma
Secondary carcinoma
1 0 1 9.0E-03 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis
1 0 1 9.0E-03 0 0
CUI: C0153618
Disease: Malignant tumor of renal pelvis
Malignant tumor of renal pelvis
1 0 1 9.0E-03 0 0
CUI: C0154064
Disease: Carcinoma in situ of anus
Carcinoma in situ of anus
1 0 1 9.0E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers
1 0 1 9.0E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe
1 0 1 9.0E-03 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle
1 0 1 9.0E-03 0 0
CUI: C0178282
Disease: Hernia of abdominal cavity
Hernia of abdominal cavity
1 0 1 9.0E-03 0 0
Hereditary Opalescent Dentin (disorder)
1 0 1 9.0E-03 0 0
CUI: C0233643
Disease: Incoherent thinking
Incoherent thinking
1 0 1 9.0E-03 0 0