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: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 5.9E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 5.9E-02 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 5.9E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 5.9E-02 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 5.9E-02 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 5.9E-02 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 5.9E-02 0 0
CUI: C0268543
Disease: Hyperammonemia, type III
Hyperammonemia, type III 		1 0 1 5.9E-02 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 5.9E-02 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 5.9E-02 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous 		1 0 1 5.9E-02 0 0
CUI: C0342608
Disease: Amyloid Polyneuropathy, British Type (disorder)
Amyloid Polyneuropathy, British Type (disorder) 		1 0 1 5.9E-02 0 0
CUI: C0392180
Disease: Necrosis of placenta
Necrosis of placenta 		1 0 1 5.9E-02 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis 		1 0 1 5.9E-02 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis 		1 0 1 5.9E-02 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 5.9E-02 0 0
CUI: C1263739
Disease: Disorder of organic acid metabolism
Disorder of organic acid metabolism 		1 0 1 5.9E-02 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 5.9E-02 0 0
CUI: C1392110
Disease: Crystalline cataract
Crystalline cataract 		1 0 1 5.9E-02 0 0
CUI: C1527337
Disease: Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Appalachian Type 		1 0 1 5.9E-02 0 0
CUI: C1837023
Disease: CATARACT, CONGENITAL, CERULEAN TYPE, 3
CATARACT, CONGENITAL, CERULEAN TYPE, 3 		1 0 1 5.9E-02 0 0
CUI: C1850039
Disease: Pericardial Effusion, Chronic
Pericardial Effusion, Chronic 		1 0 1 5.9E-02 0 0
CUI: C1855115
Disease: Methylmalonic Aciduria, mut(0) Type
Methylmalonic Aciduria, mut(0) Type 		1 0 1 5.9E-02 0 0
CUI: C1855116
Disease: Methylmalonic Aciduria, mut(-) Type
Methylmalonic Aciduria, mut(-) Type 		1 0 1 5.9E-02 0 0
CUI: C1859499
Disease: 3-methylcrotonyl CoA carboxylase 2 deficiency
3-methylcrotonyl CoA carboxylase 2 deficiency 		1 0 1 5.9E-02 0 0