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: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 2 0.50 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis 		2 1 2 0.50 1 0.25
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 0.25 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 0.25 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		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: C0423122
Disease: Ptosis of eyebrow
Ptosis of eyebrow 		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: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 0.25 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 0.25 0 0
CUI: C1960561
Disease: Hemidystonia
Hemidystonia 		1 0 1 0.25 0 0
CUI: C2750824
Disease: Dystransthyretinemic Euthyroidal Hyperthyroxinemia
Dystransthyretinemic Euthyroidal Hyperthyroxinemia 		1 0 1 0.25 0 0
CUI: C2751493
Disease: Cerebral Amyloid Angiopathy, Gsn-Related
Cerebral Amyloid Angiopathy, Gsn-Related 		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: C4024784
Disease: Amyloid deposition in the vitreous humor
Amyloid deposition in the vitreous humor 		1 0 1 0.25 0 0
CUI: C4275067
Disease: Transthyretin related familial amyloid cardiomyopathy
Transthyretin related familial amyloid cardiomyopathy 		1 0 1 0.25 0 0