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: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced
1 0 1 3.6E-02 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum
1 0 1 3.6E-02 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis
1 0 1 3.6E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases
1 0 1 3.6E-02 0 0
CUI: C0085740
Disease: Mendelson Syndrome
Mendelson Syndrome
1 0 1 3.6E-02 0 0
CUI: C0155568
Disease: Rheumatic aortic regurgitation
Rheumatic aortic regurgitation
1 0 1 3.6E-02 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast
1 0 1 3.6E-02 0 0
CUI: C0156353
Disease: Uterovaginal prolapse
Uterovaginal prolapse
1 0 1 3.6E-02 0 0
CUI: C0221745
Disease: Depression suicidal
Depression suicidal
1 0 1 3.6E-02 0 0
CUI: C0232474
Disease: Increased peristalsis
Increased peristalsis
1 0 1 3.6E-02 0 0
Subendocardial myocardial infarction
1 0 1 3.6E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark
1 0 1 3.6E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia
1 0 1 3.6E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip
1 0 1 3.6E-02 0 0
CUI: C0268796
Disease: Arteriolar nephrosclerosis
Arteriolar nephrosclerosis
1 0 1 3.6E-02 0 0
CUI: C0272256
Disease: Solitary Osseous Plasmacytoma
Solitary Osseous Plasmacytoma
1 0 1 3.6E-02 0 0
Stage I Ovarian Cancer AJCC v6 and v7
1 0 1 3.6E-02 0 0
Malignant Childhood Hemangiopericytoma
1 0 1 3.6E-02 0 0
CUI: C0281967
Disease: Retinal infarction
Retinal infarction
1 0 1 3.6E-02 0 0
CUI: C0332561
Disease: Fibrous nodule
Fibrous nodule
1 0 1 3.6E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation
1 0 1 3.6E-02 0 0
CUI: C0334542
Disease: Hemangiopericytoma, Malignant
Hemangiopericytoma, Malignant
1 0 1 3.6E-02 0 0
CUI: C0343263
Disease: Chondrolysis of articular cartilage
Chondrolysis of articular cartilage
1 0 1 3.6E-02 0 0
Primary Melanocytic Lesion of Meninges
1 0 1 3.6E-02 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder)
1 0 1 3.6E-02 0 0