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: C0026708
Disease: Mucopolysaccharidosis V
Mucopolysaccharidosis V
0 16 0 0 2 0.12
CUI: C0086431
Disease: Hurler-Scheie Syndrome
Hurler-Scheie Syndrome
0 20 0 0 1 4.8E-02
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula
1 0 1 1.2E-02 0 0
CUI: C0006264
Disease: Bronchial Neoplasms
Bronchial Neoplasms
1 0 1 1.2E-02 0 0
CUI: C0011871
Disease: Diabetic peripheral angiopathy
Diabetic peripheral angiopathy
1 0 1 1.2E-02 0 0
CUI: C0013426
Disease: Dystrophy of vulva
Dystrophy of vulva
1 0 1 1.2E-02 0 0
CUI: C0015263
Disease: Bronchospasm, Exercise-Induced
Bronchospasm, Exercise-Induced
1 0 1 1.2E-02 0 0
CUI: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome
1 0 1 1.2E-02 0 0
CUI: C0029291
Disease: Psittacosis
Psittacosis
1 0 1 1.2E-02 0 0
CUI: C0030470
Disease: Paranasal Sinus Neoplasms
Paranasal Sinus Neoplasms
1 0 1 1.2E-02 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome
1 0 1 1.2E-02 0 0
CUI: C0037942
Disease: Spinal Osteophytosis
Spinal Osteophytosis
1 0 1 1.2E-02 0 0
Undifferentiated somatoform disorder
1 0 1 1.2E-02 0 0
CUI: C0085668
Disease: Secondary carcinoma
Secondary carcinoma
1 0 1 1.2E-02 0 0
Megaloblastic anemia due to folate deficiency
1 0 1 1.2E-02 0 0
CUI: C0151536
Disease: Stenosis of bronchus
Stenosis of bronchus
1 0 1 1.2E-02 0 0
CUI: C0151686
Disease: Growth retardation
Growth retardation
1 0 1 1.2E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy
1 0 1 1.2E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen
1 0 1 1.2E-02 0 0
CUI: C0155411
Disease: Exostosis of external ear canal
Exostosis of external ear canal
1 0 1 1.2E-02 0 0
CUI: C0155761
Disease: Hyperplasia of renal artery
Hyperplasia of renal artery
1 0 1 1.2E-02 0 0
CUI: C0156245
Disease: Unilateral small kidney
Unilateral small kidney
1 0 1 1.2E-02 0 0
CUI: C0156318
Disease: Fibrosclerosis of breast
Fibrosclerosis of breast
1 0 1 1.2E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly
1 0 1 1.2E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement
1 0 1 1.2E-02 0 0