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: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive
91 0 30 0.22 0 0
Increased circulating gonadotropin level
34 0 17 0.19 0 0
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
168 88 31 0.15 2 2.1E-02
Congenital absence of germinal epithelium of testes
82 0 18 0.13 0 0
CUI: C0004509
Disease: Azoospermia
Azoospermia
254 0 34 0.12 0 0
CUI: C0241355
Disease: Small testicle
Small testicle
129 0 17 9.1E-02 0 0
CUI: C0028960
Disease: Oligospermia
Oligospermia
217 0 24 9.0E-02 0 0
Congenital bilateral aplasia of vas deferens
27 210 8 8.6E-02 7 3.3E-02
Klinefelter's syndrome - male with more than two X chromosomes
90 0 10 6.5E-02 0 0
CUI: C0021364
Disease: Male infertility
Male infertility
516 146 32 5.7E-02 1 6.5E-03
CUI: C2919755
Disease: Testicular dysgenesis syndrome
Testicular dysgenesis syndrome
19 0 5 5.7E-02 0 0
CUI: C0023601
Disease: Leydig Cell Tumor
Leydig Cell Tumor
42 0 6 5.5E-02 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome
150 0 11 5.2E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 6 5.1E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma
34 0 5 4.9E-02 0 0
CUI: C0334409
Disease: Leydig cell tumor, benign
Leydig cell tumor, benign
18 0 4 4.5E-02 0 0
CUI: C3839507
Disease: Diminished ovarian reserve
Diminished ovarian reserve
43 0 5 4.5E-02 0 0
CUI: C0016034
Disease: Breast Fibrocystic Disease
Breast Fibrocystic Disease
114 0 8 4.4E-02 0 0
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
333 0 17 4.4E-02 0 0
CUI: C0848676
Disease: Subfertility, Male
Subfertility, Male
70 0 6 4.3E-02 0 0
Elevated circulating luteinizing hormone level
23 0 4 4.3E-02 0 0
CUI: C0042341
Disease: Varicocele
Varicocele
99 0 7 4.2E-02 0 0
Elevated circulating follicle stimulating hormone level
26 0 4 4.2E-02 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder)
27 0 4 4.1E-02 0 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis
53 0 5 4.1E-02 0 0