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: C0262417
Disease: Acute on chronic pancreatitis
Acute on chronic pancreatitis
0 7 0 0 1 5.7E-03
CUI: C0029307
Disease: Oroya Fever
Oroya Fever
1 0 1 3.7E-02 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia
1 0 1 3.7E-02 0 0
CUI: C0038834
Disease: Superior Vena Cava Thrombosis
Superior Vena Cava Thrombosis
1 0 1 3.7E-02 0 0
CUI: C0042850
Disease: Vitamin B Deficiency
Vitamin B Deficiency
1 0 1 3.7E-02 0 0
Familial amyloid polyneuropathy, type VI
1 0 1 3.7E-02 0 0
Familial Amyloid Polyneuropathy, Jewish Type
1 0 1 3.7E-02 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type
1 0 1 3.7E-02 0 0
CUI: C0275584
Disease: Cutaneous nocardiosis
Cutaneous nocardiosis
1 0 1 3.7E-02 0 0
CUI: C0334337
Disease: Endometrioid adenoma
Endometrioid adenoma
1 0 1 3.7E-02 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous
1 0 1 3.7E-02 0 0
Amyloid Polyneuropathy, British Type (disorder)
1 0 1 3.7E-02 0 0
CUI: C0399356
Disease: Supernumerary cusp
Supernumerary cusp
1 0 1 3.7E-02 0 0
Type 2 diabetes mellitus without complication
1 0 1 3.7E-02 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis
1 0 1 3.7E-02 0 0
CUI: C0559523
Disease: Genital tuberculosis
Genital tuberculosis
1 0 1 3.7E-02 0 0
CUI: C0597966
Disease: Juxtaglomerular cell hyperplasia
Juxtaglomerular cell hyperplasia
1 0 1 3.7E-02 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis
1 0 1 3.7E-02 0 0
CUI: C0749474
Disease: thyroid nodule solitary
thyroid nodule solitary
1 0 1 3.7E-02 0 0
CUI: C0948075
Disease: Anal infection
Anal infection
1 0 1 3.7E-02 0 0
CUI: C1096485
Disease: Haemophilia A with anti factor VIII
Haemophilia A with anti factor VIII
1 0 1 3.7E-02 0 0
CUI: C1336109
Disease: Stage IA1 Cervical Cancer
Stage IA1 Cervical Cancer
1 0 1 3.7E-02 0 0
Allergic disorder of respiratory system
1 0 1 3.7E-02 0 0
Familial Amyloid Polyneuropathy, Appalachian Type
1 0 1 3.7E-02 0 0
Spastic paraplegia 13, autosomal dominant
1 0 1 3.7E-02 0 0