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: C4049281
Disease: Pseudogynaecomastia
Pseudogynaecomastia
2 0 2 0.25 0 0
CUI: C1274999
Disease: Skin flap necrosis
Skin flap necrosis
5 0 2 0.18 0 0
CUI: C4072885
Disease: Increased serum testosterone level
Increased serum testosterone level
5 0 2 0.18 0 0
CUI: C0149741
Disease: nipple discharge
nipple discharge
7 0 2 0.15 0 0
Tyrosine Transaminase Deficiency Disease
7 0 2 0.15 0 0
CUI: C1850325
Disease: Labial hypoplasia
Labial hypoplasia
7 0 2 0.15 0 0
CUI: C0452148
Disease: Hypospadias, perineal
Hypospadias, perineal
8 0 2 0.14 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism
1 0 1 0.12 0 0
CUI: C0017412
Disease: Genital Diseases, Male
Genital Diseases, Male
1 0 1 0.12 0 0
CUI: C0220761
Disease: Dizygotic twins (disorder)
Dizygotic twins (disorder)
1 0 1 0.12 0 0
CUI: C0233200
Disease: Cullen's sign
Cullen's sign
1 0 1 0.12 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia
1 0 1 0.12 0 0
Disorder of male reproductive system
1 0 1 0.12 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism
1 0 1 0.12 0 0
Mullerian inhibiting factor deficiency
1 0 1 0.12 0 0
Incomplete testicular feminization syndrome
1 0 1 0.12 0 0
CUI: C0404562
Disease: Incipient ovarian failure
Incipient ovarian failure
1 0 1 0.12 0 0
CUI: C0406482
Disease: Nodulocystic acne
Nodulocystic acne
1 0 1 0.12 0 0
CUI: C0546393
Disease: Macular cutaneous amyloidosis
Macular cutaneous amyloidosis
1 0 1 0.12 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome
1 0 1 0.12 0 0
CUI: C0752353
Disease: Atrophy, Muscular, Spinobulbar
Atrophy, Muscular, Spinobulbar
1 0 1 0.12 0 0
CUI: C0860159
Disease: Partial androgen resistance
Partial androgen resistance
1 0 1 0.12 0 0
CUI: C0865181
Disease: Female Virilization
Female Virilization
1 0 1 0.12 0 0
CUI: C1280777
Disease: displaced uterus
displaced uterus
1 0 1 0.12 0 0
Increased capillary permeability (finding)
1 0 1 0.12 0 0