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: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome 		5 0 2 0.29 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 0.25 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 0.25 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 0.25 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 0.25 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous 		1 0 1 0.25 0 0
CUI: C0342608
Disease: Amyloid Polyneuropathy, British Type (disorder)
Amyloid Polyneuropathy, British Type (disorder) 		1 0 1 0.25 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis 		1 0 1 0.25 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis 		1 0 1 0.25 0 0
CUI: C1527337
Disease: Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Appalachian Type 		1 0 1 0.25 0 0
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 0.25 0 0
CUI: C2750824
Disease: Dystransthyretinemic Euthyroidal Hyperthyroxinemia
Dystransthyretinemic Euthyroidal Hyperthyroxinemia 		1 0 1 0.25 0 0
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED 		1 0 1 0.25 0 0
CUI: C3151471
Disease: AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED 		1 0 1 0.25 0 0
CUI: C3468338
Disease: CARPAL TUNNEL SYNDROME, FAMILIAL
CARPAL TUNNEL SYNDROME, FAMILIAL 		1 0 1 0.25 0 0
CUI: C3864035
Disease: Bilateral carpal tunnel syndrome
Bilateral carpal tunnel syndrome 		1 0 1 0.25 0 0
CUI: C4014310
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 		1 0 1 0.25 0 0
CUI: C4014962
Disease: FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG 		1 1 1 0.25 1 4.2E-02
CUI: C4024784
Disease: Amyloid deposition in the vitreous humor
Amyloid deposition in the vitreous humor 		1 0 1 0.25 0 0
CUI: C4274078
Disease: Hyperinsulinism due to HNF4A deficiency
Hyperinsulinism due to HNF4A deficiency 		1 3 1 0.25 1 3.8E-02
CUI: C4275067
Disease: Transthyretin related familial amyloid cardiomyopathy
Transthyretin related familial amyloid cardiomyopathy 		1 0 1 0.25 0 0
CUI: C4303475
Disease: Hyperinsulinism due to HNF1A deficiency
Hyperinsulinism due to HNF1A deficiency 		1 0 1 0.25 0 0
CUI: C1838100
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder) 		12 0 3 0.23 0 0
CUI: C0015938
Disease: Fetal Macrosomia
Fetal Macrosomia 		2 0 1 0.20 0 0
CUI: C0158328
Disease: Trigger Finger Disorder
Trigger Finger Disorder 		2 0 1 0.20 0 0