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: C0393911
Disease: Pure Autonomic Failure
Pure Autonomic Failure
12 0 3 8.3E-02 0 0
CUI: C0398691
Disease: Hyperimmunoglobulinemia D
Hyperimmunoglobulinemia D
12 0 3 8.3E-02 0 0
CUI: C1704417
Disease: Hyperlipoproteinemia Type IIb
Hyperlipoproteinemia Type IIb
25 0 4 8.3E-02 0 0
CUI: C0311276
Disease: Severe malnutrition
Severe malnutrition
13 0 3 8.1E-02 0 0
CUI: C0158026
Disease: Monoarthritis
Monoarthritis
14 0 3 7.9E-02 0 0
CUI: C0085624
Disease: Burning sensation
Burning sensation
30 0 4 7.5E-02 0 0
Orthostatic hypotension due to autonomic dysfunction
16 0 3 7.5E-02 0 0
CUI: C0039292
Disease: Tangier Disease
Tangier Disease
31 0 4 7.4E-02 0 0
CUI: C0234906
Disease: Annular Erythema
Annular Erythema
2 0 2 7.4E-02 0 0
Familial Amyloid Polyneuropathy, Type IV
2 0 2 7.4E-02 0 0
CUI: C1142436
Disease: Sundowning
Sundowning
2 0 2 7.4E-02 0 0
CUI: C1719315
Disease: Hereditary cardiac amyloidosis
Hereditary cardiac amyloidosis
2 0 2 7.4E-02 0 0
CUI: C1719316
Disease: Inherited systemic amyloidosis
Inherited systemic amyloidosis
2 0 2 7.4E-02 0 0
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia
17 0 3 7.3E-02 0 0
CUI: C0151859
Disease: Polyserositis
Polyserositis
3 0 2 7.1E-02 0 0
CUI: C0206247
Disease: Amyloid Neuropathies
Amyloid Neuropathies
3 3 2 7.1E-02 1 8.3E-02
CUI: C0281774
Disease: Acute psychosis
Acute psychosis
3 0 2 7.1E-02 0 0
CUI: C0519002
Disease: Gastrointestinal amyloidosis
Gastrointestinal amyloidosis
3 0 2 7.1E-02 0 0
CUI: C0678201
Disease: Terminal Ileitis
Terminal Ileitis
3 0 2 7.1E-02 0 0
Iatrogenic Jakob-Creutzfeldt disease
3 0 2 7.1E-02 0 0
CUI: C3494360
Disease: Prodromal Period
Prodromal Period
3 0 2 7.1E-02 0 0
CUI: C3804968
Disease: Pathergy reaction
Pathergy reaction
3 0 2 7.1E-02 0 0
CUI: C3829514
Disease: Intrapartum fever
Intrapartum fever
3 0 2 7.1E-02 0 0
CUI: C4274343
Disease: Solitary rectal ulcer syndrome
Solitary rectal ulcer syndrome
3 0 2 7.1E-02 0 0
CUI: C4509023
Disease: Light chain (AL) amyloidosis
Light chain (AL) amyloidosis
3 0 2 7.1E-02 0 0