Source: BEFREE ×
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: C1261504
Disease: Congenital absence of both testes
Congenital absence of both testes 		3 0 2 0.15 0 0
CUI: C4551490
Disease: Ovotestis
Ovotestis 		3 0 2 0.15 0 0
CUI: C0268301
Disease: Reifenstein Syndrome
Reifenstein Syndrome 		11 0 3 0.15 0 0
CUI: C2930618
Disease: Intersex Conditions
Intersex Conditions 		4 0 2 0.14 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		5 0 2 0.13 0 0
CUI: C0242526
Disease: Gonadal Dysgenesis, 45,X
Gonadal Dysgenesis, 45,X 		19 0 3 0.11 0 0
CUI: C0266360
Disease: Streak gonad
Streak gonad 		9 0 2 0.11 0 0
CUI: C0432475
Disease: XX males
XX males 		30 0 4 0.11 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		21 0 3 1.0E-01 0 0
CUI: C0265309
Disease: Leri-Weill dyschondrosteosis
Leri-Weill dyschondrosteosis 		10 0 2 1.0E-01 0 0
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea 		11 0 2 9.5E-02 0 0
CUI: C2936419
Disease: 46, XX Testicular Disorders of Sex Development
46, XX Testicular Disorders of Sex Development 		11 0 2 9.5E-02 0 0
CUI: C0029928
Disease: Ovarian Diseases
Ovarian Diseases 		12 0 2 9.1E-02 0 0
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism 		26 0 3 8.6E-02 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 8.3E-02 0 0
CUI: C0018051
Disease: Gonadal Dysgenesis
Gonadal Dysgenesis 		27 0 3 8.3E-02 0 0
CUI: C0026210
Disease: Mirror Writing
Mirror Writing 		1 0 1 8.3E-02 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 8.3E-02 0 0
CUI: C0158465
Disease: Acquired cubitus valgus
Acquired cubitus valgus 		1 0 1 8.3E-02 0 0
CUI: C0270709
Disease: Rud Syndrome
Rud Syndrome 		1 0 1 8.3E-02 0 0
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		1 0 1 8.3E-02 0 0
CUI: C0271629
Disease: Mullerian inhibiting factor deficiency
Mullerian inhibiting factor deficiency 		1 0 1 8.3E-02 0 0
CUI: C0375536
Disease: Congenital osteodystrophy
Congenital osteodystrophy 		1 0 1 8.3E-02 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 8.3E-02 0 0
CUI: C0404562
Disease: Incipient ovarian failure
Incipient ovarian failure 		1 0 1 8.3E-02 0 0