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: C0013473
Disease: Eating Disorders
Eating Disorders
1 0 1 5.0E-02 0 0
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
2 0 2 1.0E-01 0 0
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
2 0 2 1.0E-01 0 0
Anti-cyclic citrullinated peptide antibody
2 0 2 1.0E-01 0 0
CUI: C0024299
Disease: Lymphoma
Lymphoma
4 0 1 4.3E-02 0 0
CUI: C0202083
Disease: Immunoglobulin A measurement
Immunoglobulin A measurement
4 0 2 9.1E-02 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
4 0 3 0.14 0 0
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
5 0 1 4.2E-02 0 0
Chemical and Drug Induced Liver Injury
5 0 3 0.14 0 0
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
6 23 4 0.18 2 2.8E-03
CUI: C0201910
Disease: Beta-2-microglobulin measurement
Beta-2-microglobulin measurement
6 0 2 8.3E-02 0 0
CUI: C4048328
Disease: cervical cancer
cervical cancer
6 0 1 4.0E-02 0 0
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
7 22 4 0.17 1 1.4E-03
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
7 0 1 3.8E-02 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
9 25 2 7.4E-02 1 1.4E-03
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
9 0 2 7.4E-02 0 0
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
9 0 2 7.4E-02 0 0
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
11 42 1 3.3E-02 2 2.7E-03
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
12 0 4 0.14 0 0
CUI: C0023343
Disease: Leprosy
Leprosy
13 0 3 1.0E-01 0 0
Activated Partial Thromboplastin Time measurement
13 0 2 6.5E-02 0 0
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
14 0 2 6.2E-02 0 0
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
15 0 2 6.1E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome
17 0 2 5.7E-02 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
17 0 2 5.7E-02 0 0