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: C2936694
Disease: Swyer Syndrome
Swyer Syndrome
17 0 7 0.33 0 0
CUI: C0936016
Disease: Testicular Feminization
Testicular Feminization
24 0 6 0.21 0 0
CUI: C4048549
Disease: Malignant germ cell neoplasm
Malignant germ cell neoplasm
7 0 3 0.20 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma
34 0 7 0.18 0 0
CUI: C0432481
Disease: 46, XX true hermaphrodite
46, XX true hermaphrodite
2 0 2 0.18 0 0
CUI: C0018054
Disease: Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis, 46,XY
29 0 6 0.18 0 0
CUI: C1266157
Disease: Intratubular malignant germ cells
Intratubular malignant germ cells
16 0 4 0.17 0 0
CUI: C0687149
Disease: Pure gonadal dysgenesis
Pure gonadal dysgenesis
4 0 2 0.15 0 0
CUI: C4040907
Disease: Mosaic Turner syndrome
Mosaic Turner syndrome
4 0 2 0.15 0 0
CUI: C0242526
Disease: Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, 45,X
23 0 4 0.13 0 0
CUI: C0333693
Disease: Triploidy syndrome
Triploidy syndrome
42 0 6 0.13 0 0
CUI: C1507149
Disease: Partial chromosome Y deletion
Partial chromosome Y deletion
8 0 2 0.12 0 0
Male sterility due to Y-chromosome deletions
8 0 2 0.12 0 0
CUI: C0036769
Disease: Sertoli Cell Tumor
Sertoli Cell Tumor
9 0 2 0.11 0 0
CUI: C0036875
Disease: Disorders of Sex Development
Disorders of Sex Development
39 0 5 0.11 0 0
CUI: C0266360
Disease: Streak gonad
Streak gonad
9 0 2 0.11 0 0
CUI: C0452147
Disease: Hypospadias, penoscrotal
Hypospadias, penoscrotal
9 0 2 0.11 0 0
CUI: C0013377
Disease: Dysgerminoma
Dysgerminoma
42 0 5 0.10 0 0
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome
11 0 2 1.0E-01 0 0
46, XX Testicular Disorders of Sex Development
11 0 2 1.0E-01 0 0
CUI: C0856151
Disease: Fat redistribution
Fat redistribution
12 0 2 9.5E-02 0 0
CUI: C1515283
Disease: Testicular gonadoblastoma
Testicular gonadoblastoma
12 0 2 9.5E-02 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male
1 0 1 9.1E-02 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype
1 0 1 9.1E-02 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia
1 0 1 9.1E-02 0 0