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: C1306889
Disease: Peripheral arterial occlusive disease
Peripheral arterial occlusive disease 		35 0 4 6.2E-02 0 0
CUI: C1260880
Disease: Rhinorrhea
Rhinorrhea 		19 0 3 6.1E-02 0 0
CUI: C1261287
Disease: Stenosis
Stenosis 		19 0 3 6.1E-02 0 0
CUI: C0856874
Disease: Subclinical diabetes
Subclinical diabetes 		2 0 2 6.1E-02 0 0
CUI: C0936273
Disease: Familial Amyloid Polyneuropathy, Type IV
Familial Amyloid Polyneuropathy, Type IV 		2 0 2 6.1E-02 0 0
CUI: C1719315
Disease: Hereditary cardiac amyloidosis
Hereditary cardiac amyloidosis 		2 1 2 6.1E-02 1 5.3E-02
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis 		2 0 2 6.1E-02 0 0
CUI: C1854380
Disease: NEMALINE MYOPATHY 5
NEMALINE MYOPATHY 5 		2 0 2 6.1E-02 0 0
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias 		20 0 3 6.0E-02 0 0
CUI: C3888896
Disease: Wet age-related macular degeneration
Wet age-related macular degeneration 		20 0 3 6.0E-02 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis 		38 0 4 6.0E-02 0 0
CUI: C0162279
Disease: Choroidal detachment
Choroidal detachment 		3 0 2 5.9E-02 0 0
CUI: C0206247
Disease: Amyloid Neuropathies
Amyloid Neuropathies 		3 3 2 5.9E-02 2 1.0E-01
CUI: C0267842
Disease: Acute cholecystitis without calculus
Acute cholecystitis without calculus 		3 0 2 5.9E-02 0 0
CUI: C0393578
Disease: Pallidoluysian degeneration
Pallidoluysian degeneration 		3 0 2 5.9E-02 0 0
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal 		3 0 2 5.9E-02 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 3 5.9E-02 0 0
CUI: C1394290
Disease: Cyanotic heart disease
Cyanotic heart disease 		3 0 2 5.9E-02 0 0
CUI: C3495426
Disease: Homocysteinemia
Homocysteinemia 		21 0 3 5.9E-02 0 0
CUI: C4509024
Disease: Senile systemic amyloidosis (SSA)
Senile systemic amyloidosis (SSA) 		3 1 2 5.9E-02 1 5.3E-02
CUI: C4551500
Disease: Amyloid Polyneuropathy, Iowa Type
Amyloid Polyneuropathy, Iowa Type 		3 0 2 5.9E-02 0 0
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
Cholesteryl Ester Transfer Protein Deficiency 		22 0 3 5.8E-02 0 0
CUI: C0014849
Disease: Esophageal and Gastric Varices
Esophageal and Gastric Varices 		4 0 2 5.7E-02 0 0
CUI: C0021296
Disease: Infant, Small for Gestational Age
Infant, Small for Gestational Age 		4 0 2 5.7E-02 0 0
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis 		41 11 4 5.7E-02 1 3.4E-02