Source: ALL
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: C0152516
Disease: Bacterial enteritis
Bacterial enteritis 		1 0 1 0.11 0 0
CUI: C0154007
Disease: Benign neoplasm of testis
Benign neoplasm of testis 		1 0 1 0.11 0 0
CUI: C0265323
Disease: Peutz-Jeghers polyps of small bowel
Peutz-Jeghers polyps of small bowel 		1 0 1 0.11 0 0
CUI: C0275553
Disease: Bacterial cholangitis
Bacterial cholangitis 		1 0 1 0.11 0 0
CUI: C0406425
Disease: Laugier-Hunziker syndrome
Laugier-Hunziker syndrome 		1 0 1 0.11 0 0
CUI: C0406814
Disease: Labial lentigo
Labial lentigo 		1 0 1 0.11 0 0
CUI: C0456487
Disease: Peutz Jehgers polyp
Peutz Jehgers polyp 		1 0 1 0.11 0 0
CUI: C0496924
Disease: Neoplasm of uncertain or unknown behavior of testis
Neoplasm of uncertain or unknown behavior of testis 		1 0 1 0.11 0 0
CUI: C1142307
Disease: Paratubal Cyst
Paratubal Cyst 		1 0 1 0.11 0 0
CUI: C1832471
Disease: Renal dysplasia diffuse cystic
Renal dysplasia diffuse cystic 		1 0 1 0.11 0 0
CUI: C1853153
Disease: JOUBERT SYNDROME 6
JOUBERT SYNDROME 6 		1 0 1 0.11 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch 		1 0 1 0.11 0 0
CUI: C1865616
Disease: HEMOCHROMATOSIS, TYPE 2B
HEMOCHROMATOSIS, TYPE 2B 		1 0 1 0.11 0 0
CUI: C1866053
Disease: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Congenital Heart Defects, and Posterior Embryotoxon 		1 0 1 0.11 0 0
CUI: C1868007
Disease: Precocious puberty with Sertoli cell tumor
Precocious puberty with Sertoli cell tumor 		1 0 1 0.11 0 0
CUI: C1963822
Disease: Mucosal pigmentation
Mucosal pigmentation 		1 0 1 0.11 0 0
CUI: C1969052
Disease: MECKEL SYNDROME, TYPE 5
MECKEL SYNDROME, TYPE 5 		1 0 1 0.11 0 0
CUI: C1969053
Disease: JOUBERT SYNDROME 7
JOUBERT SYNDROME 7 		1 0 1 0.11 0 0
CUI: C2676788
Disease: JOUBERT SYNDROME 9 (disorder)
JOUBERT SYNDROME 9 (disorder) 		1 0 1 0.11 0 0
CUI: C2676790
Disease: MECKEL SYNDROME, TYPE 6 (disorder)
MECKEL SYNDROME, TYPE 6 (disorder) 		1 0 1 0.11 0 0
CUI: C3150796
Disease: NEPHRONOPHTHISIS 11
NEPHRONOPHTHISIS 11 		1 0 1 0.11 0 0
CUI: C3489571
Disease: Familial Extrahepatic Biliary Atresia
Familial Extrahepatic Biliary Atresia 		1 0 1 0.11 0 0
CUI: C3489572
Disease: Idiopathic Extrahepatic Biliary Atresia
Idiopathic Extrahepatic Biliary Atresia 		1 0 1 0.11 0 0
CUI: C4017203
Disease: BARDET-BIEDL SYNDROME 14, MODIFIER OF
BARDET-BIEDL SYNDROME 14, MODIFIER OF 		1 0 1 0.11 0 0
CUI: C4020959
Disease: Abnormal pigmentation of the oral mucosa
Abnormal pigmentation of the oral mucosa 		1 0 1 0.11 0 0