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 36 4.9E-02 26 0.19
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis 		33 19 16 2.3E-02 13 0.13
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy 		156 32 40 4.9E-02 13 0.12
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		15 16 13 1.9E-02 8 7.9E-02
CUI: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis 		21 10 19 2.7E-02 7 7.3E-02
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis 		27 10 25 3.6E-02 7 7.3E-02
CUI: C0264694
Disease: Chronic myocardial ischemia
Chronic myocardial ischemia 		29 7 10 1.4E-02 6 6.4E-02
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		20 7 18 2.6E-02 6 6.4E-02
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		19 12 15 2.1E-02 6 6.1E-02
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		549 69 119 0.11 9 5.9E-02
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		65 22 48 6.8E-02 6 5.5E-02
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		351 81 93 9.8E-02 9 5.5E-02
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever 		133 82 62 8.1E-02 9 5.4E-02
CUI: C3151470
Disease: AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED 		1 5 1 1.4E-03 5 5.4E-02
CUI: C0007286
Disease: Carpal Tunnel Syndrome
Carpal Tunnel Syndrome 		87 46 26 3.4E-02 7 5.3E-02
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 276 190 0.12 18 5.1E-02
CUI: C2936349
Disease: Plaque, Amyloid
Plaque, Amyloid 		123 10 79 0.11 5 5.1E-02
CUI: C0007682
Disease: CNS disorder
CNS disorder 		319 11 105 0.12 5 5.1E-02
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders 		1515 85 351 0.19 7 4.1E-02
CUI: C1851347
Disease: Familial Mediterranean Fever, Autosomal Dominant
Familial Mediterranean Fever, Autosomal Dominant 		1 9 1 1.4E-03 4 4.1E-02
CUI: C0276496
Disease: Familial Alzheimer Disease (FAD)
Familial Alzheimer Disease (FAD) 		260 95 125 0.15 7 3.9E-02
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		8 15 7 1.0E-02 4 3.8E-02
CUI: C0233794
Disease: Memory impairment
Memory impairment 		763 48 254 0.21 5 3.7E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 50 41 3.9E-02 5 3.6E-02
CUI: C1628319
Disease: Lattice corneal dystrophy Type II
Lattice corneal dystrophy Type II 		4 4 4 5.8E-03 3 3.2E-02