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: C0206247
Disease: Amyloid Neuropathies
Amyloid Neuropathies 		3 0 2 0.40 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 0 2 0.40 0 0
CUI: C0019640
Disease: Histomoniasis
Histomoniasis 		1 0 1 0.25 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 0.25 0 0
CUI: C0037974
Disease: Spirochaetales Infections
Spirochaetales Infections 		1 0 1 0.25 0 0
CUI: C0152902
Disease: Tuberculosis of esophagus
Tuberculosis of esophagus 		1 0 1 0.25 0 0
CUI: C0234959
Disease: Panarteritis
Panarteritis 		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: C0268757
Disease: SLE glomerulonephritis syndrome, WHO class IV
SLE glomerulonephritis syndrome, WHO class IV 		1 0 1 0.25 0 0
CUI: C0271271
Disease: Xerotic keratitis
Xerotic keratitis 		1 0 1 0.25 0 0
CUI: C0275959
Disease: Acute tuberculosis
Acute tuberculosis 		1 0 1 0.25 0 0
CUI: C0276196
Disease: Goatpox
Goatpox 		1 0 1 0.25 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous 		1 0 1 0.25 0 0
CUI: C0341117
Disease: Esophageal erosions
Esophageal erosions 		1 0 1 0.25 0 0
CUI: C0341702
Disease: Acquired Fanconi syndrome
Acquired Fanconi syndrome 		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: C0343400
Disease: Intestinal microsporidiosis
Intestinal microsporidiosis 		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: C0854406
Disease: Chronic proliferative glomerulonephritis
Chronic proliferative glomerulonephritis 		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: C1697744
Disease: HIV peripheral neuropathy
HIV peripheral neuropathy 		1 0 1 0.25 0 0
CUI: C1836023
Disease: Drug Metabolism, Poor, CYP2C19-Related
Drug Metabolism, Poor, CYP2C19-Related 		1 0 1 0.25 0 0