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: C0007397
Disease: Catastrophic Illness
Catastrophic Illness 		1 0 1 0.50 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 0.50 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 0.50 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 0.50 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 0.50 0 0
CUI: C0271712
Disease: Hypoglycemia of childhood
Hypoglycemia of childhood 		1 0 1 0.50 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous 		1 0 1 0.50 0 0
CUI: C0341274
Disease: Acute radiation enteritis
Acute radiation enteritis 		1 0 1 0.50 0 0
CUI: C0342608
Disease: Amyloid Polyneuropathy, British Type (disorder)
Amyloid Polyneuropathy, British Type (disorder) 		1 0 1 0.50 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis 		1 0 1 0.50 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis 		1 0 1 0.50 0 0
CUI: C1527337
Disease: Familial Amyloid Polyneuropathy, Appalachian Type
Familial Amyloid Polyneuropathy, Appalachian Type 		1 0 1 0.50 0 0
CUI: C1881406
Disease: Lipase Hypersecretion Syndrome
Lipase Hypersecretion Syndrome 		1 0 1 0.50 0 0
CUI: C2750824
Disease: Dystransthyretinemic Euthyroidal Hyperthyroxinemia
Dystransthyretinemic Euthyroidal Hyperthyroxinemia 		1 0 1 0.50 0 0
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED 		1 0 1 0.50 0 0
CUI: C3151471
Disease: AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED 		1 0 1 0.50 0 0
CUI: C3468338
Disease: CARPAL TUNNEL SYNDROME, FAMILIAL
CARPAL TUNNEL SYNDROME, FAMILIAL 		1 0 1 0.50 0 0
CUI: C3864035
Disease: Bilateral carpal tunnel syndrome
Bilateral carpal tunnel syndrome 		1 0 1 0.50 0 0
CUI: C4024784
Disease: Amyloid deposition in the vitreous humor
Amyloid deposition in the vitreous humor 		1 0 1 0.50 0 0
CUI: C4275067
Disease: Transthyretin related familial amyloid cardiomyopathy
Transthyretin related familial amyloid cardiomyopathy 		1 0 1 0.50 0 0
CUI: C4476847
Disease: Short bowel
Short bowel 		1 0 1 0.50 0 0
CUI: C0151911
Disease: Generalized Spasms
Generalized Spasms 		2 0 1 0.33 0 0
CUI: C0158328
Disease: Trigger Finger Disorder
Trigger Finger Disorder 		2 0 1 0.33 0 0
CUI: C0221243
Disease: Necrolytic Migratory Erythema
Necrolytic Migratory Erythema 		2 0 1 0.33 0 0
CUI: C0235229
Disease: Ciliary Body Spasm
Ciliary Body Spasm 		2 0 1 0.33 0 0