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: C0268380
Disease: Systemic amyloidosis
Systemic amyloidosis
21 10 9 0.28 1 6.2E-02
CUI: C0281479
Disease: Primary Systemic Amyloidosis
Primary Systemic Amyloidosis
27 10 9 0.24 1 6.2E-02
CUI: C0398691
Disease: Hyperimmunoglobulinemia D
Hyperimmunoglobulinemia D
12 0 5 0.19 0 0
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
38 10 9 0.18 1 6.2E-02
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition
6 0 4 0.18 0 0
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis
41 11 9 0.17 1 5.9E-02
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral
8 15 4 0.17 2 1.0E-01
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis
10 6 4 0.15 1 8.3E-02
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial
19 12 5 0.15 1 5.6E-02
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis
4 0 3 0.14 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis
5 0 3 0.14 0 0
CUI: C0585274
Disease: Periodic syndrome
Periodic syndrome
6 0 3 0.13 0 0
Tumor necrosis factor receptor associated periodic syndrome [TRAPS]
6 0 3 0.13 0 0
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial
15 0 4 0.13 0 0
CUI: C3889979
Disease: Periodic Fever Syndrome
Periodic Fever Syndrome
16 0 4 0.12 0 0
CUI: C0546994
Disease: Acute viral encephalitis
Acute viral encephalitis
8 0 3 0.12 0 0
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous
9 0 3 0.12 0 0
Cryopyrin-Associated Periodic Syndromes
39 0 6 0.11 0 0
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase
20 0 4 0.11 0 0
Decreased HDL cholesterol concentration
12 0 3 0.10 0 0
CUI: C0149910
Disease: Intermittent joint effusion
Intermittent joint effusion
2 0 2 1.0E-01 0 0
CUI: C0264964
Disease: Aneurysm of popliteal artery
Aneurysm of popliteal artery
2 0 2 1.0E-01 0 0
Familial non-neuropathic amyloidosis
2 0 2 1.0E-01 0 0
CUI: C1719313
Disease: Hereditary amyloid nephropathy
Hereditary amyloid nephropathy
2 0 2 1.0E-01 0 0
Psoriatic Juvenile Idiopathic Arthritis
2 0 2 1.0E-01 0 0