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: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		74 68 23 0.27 19 0.28
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		15 16 7 0.17 2 6.1E-02
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous 		9 10 4 0.11 1 3.6E-02
CUI: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis 		21 10 5 0.10 1 3.6E-02
CUI: C2718001
Disease: Protein Misfolding Disorders
Protein Misfolding Disorders 		38 0 6 9.2E-02 0 0
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis 		27 10 5 9.1E-02 1 3.6E-02
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 2 3 9.1E-02 1 5.0E-02
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 3 8.6E-02 0 0
CUI: C1536221
Disease: Non ST segment elevation myocardial infarction
Non ST segment elevation myocardial infarction 		18 0 4 8.5E-02 0 0
CUI: C0268384
Disease: Familial Amyloid Neuropathy, Portuguese Type
Familial Amyloid Neuropathy, Portuguese Type 		6 2 3 8.3E-02 1 5.0E-02
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		19 12 4 8.3E-02 1 3.3E-02
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		20 0 4 8.2E-02 0 0
CUI: C0751587
Disease: CADASIL Syndrome
CADASIL Syndrome 		40 0 5 7.4E-02 0 0
CUI: C0007775
Disease: Cerebral Atherosclerosis
Cerebral Atherosclerosis 		11 0 3 7.3E-02 0 0
CUI: C0856151
Disease: Fat redistribution
Fat redistribution 		12 0 3 7.1E-02 0 0
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III 		28 0 4 7.0E-02 0 0
CUI: C0028968
Disease: Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies 		28 0 4 7.0E-02 0 0
CUI: C0344917
Disease: Left ventricular outflow tract obstruction
Left ventricular outflow tract obstruction 		13 0 3 7.0E-02 0 0
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy 		29 7 4 6.9E-02 2 8.3E-02
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 3 6.8E-02 0 0
CUI: C1527311
Disease: Brain Edema
Brain Edema 		30 0 4 6.8E-02 0 0
CUI: C1866751
Disease: Spinocerebellar tract degeneration
Spinocerebellar tract degeneration 		15 0 3 6.7E-02 0 0
CUI: C1868528
Disease: Orthostatic hypotension due to autonomic dysfunction
Orthostatic hypotension due to autonomic dysfunction 		16 0 3 6.5E-02 0 0
CUI: C0155686
Disease: Acute myocarditis
Acute myocarditis 		33 0 4 6.5E-02 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 3 6.2E-02 0 0