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: C0235250
Disease: Hyperemesis
Hyperemesis 		3 0 1 0.33 0 0
CUI: C0342623
Disease: Senile systemic amyloidosis
Senile systemic amyloidosis 		3 0 1 0.33 0 0
CUI: C0519002
Disease: Gastrointestinal amyloidosis
Gastrointestinal amyloidosis 		3 0 1 0.33 0 0
CUI: C1266092
Disease: Thymoma, type AB
Thymoma, type AB 		3 0 1 0.33 0 0
CUI: C1839141
Disease: Thyroxine-Binding Globulin Deficiency
Thyroxine-Binding Globulin Deficiency 		3 0 1 0.33 0 0
CUI: C4509024
Disease: Senile systemic amyloidosis (SSA)
Senile systemic amyloidosis (SSA) 		3 0 1 0.33 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 2 1 0.33 1 0.50
CUI: C4551500
Disease: Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Iowa Type 		3 0 1 0.33 0 0
CUI: C0016242
Disease: Vitreous floaters
Vitreous floaters 		4 0 1 0.25 0 0
CUI: C0021296
Disease: Infant, Small for Gestational Age
Infant, Small for Gestational Age 		4 0 1 0.25 0 0
CUI: C0850149
Disease: Dry cough
Dry cough 		4 0 1 0.25 0 0
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 0 1 0.25 0 0
CUI: C1852093
Disease: Maturity-Onset Diabetes of the Young, Type 1
Maturity-Onset Diabetes of the Young, Type 1 		4 0 1 0.25 0 0
CUI: C0020551
Disease: Hyperthyroxinemia
Hyperthyroxinemia 		5 0 1 0.20 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 1 0.20 0 0
CUI: C0751448
Disease: Polyneuropathy, Familial
Polyneuropathy, Familial 		5 0 1 0.20 0 0
CUI: C1858501
Disease: Spinocerebellar Ataxia 12
Spinocerebellar Ataxia 12 		5 0 1 0.20 0 0
CUI: C2939462
Disease: Immunoglobulin deposition disease
Immunoglobulin deposition disease 		5 0 1 0.20 0 0
CUI: C3241958
Disease: Myocardial Disorder
Myocardial Disorder 		5 0 1 0.20 0 0
CUI: C0014858
Disease: Esophageal motility disorders
Esophageal motility disorders 		6 0 1 0.17 0 0
CUI: C0014863
Disease: Esophageal spasm
Esophageal spasm 		6 0 1 0.17 0 0
CUI: C0268384
Disease: Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Neuropathy, Portuguese Type 		6 0 1 0.17 0 0
CUI: C0751409
Disease: Upper Extremity Paresis
Upper Extremity Paresis 		6 0 1 0.17 0 0
CUI: C3489576
Disease: Sexual Violence
Sexual Violence 		6 0 1 0.17 0 0
CUI: C4732837
Disease: Leptomeningeal enhancement
Leptomeningeal enhancement 		6 0 1 0.17 0 0