Source: ALL
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: C0268285
Disease: Adrenal hyperplasia, congenital, type 5
Adrenal hyperplasia, congenital, type 5 		7 27 4 0.36 3 9.7E-02
CUI: C0032796
Disease: Postpartum Amenorrhea
Postpartum Amenorrhea 		6 0 3 0.27 0 0
CUI: C0242341
Disease: Sexual Infantilism
Sexual Infantilism 		2 0 2 0.25 0 0
CUI: C4024735
Disease: Maternal virilization in pregnancy
Maternal virilization in pregnancy 		2 0 2 0.25 0 0
CUI: C0271725
Disease: Iatrogenic Cushing's disease
Iatrogenic Cushing's disease 		4 0 2 0.20 0 0
CUI: C4329212
Disease: 17-Alpha-Hydroxylase/17,20 Lyase Deficiency
17-Alpha-Hydroxylase/17,20 Lyase Deficiency 		4 8 2 0.20 1 7.1E-02
CUI: C0271528
Disease: Isosexual precocious puberty
Isosexual precocious puberty 		5 0 2 0.18 0 0
CUI: C1291245
Disease: Cortisone reductase deficiency
Cortisone reductase deficiency 		5 0 2 0.18 0 0
CUI: C4021124
Disease: Adrenocorticotropic hormone excess
Adrenocorticotropic hormone excess 		5 0 2 0.18 0 0
CUI: C4024641
Disease: Enlarged polycystic ovaries
Enlarged polycystic ovaries 		18 0 4 0.18 0 0
CUI: C0342513
Disease: Idiopathic hirsutism
Idiopathic hirsutism 		12 0 3 0.18 0 0
CUI: C1860042
Disease: Antley-Bixler Syndrome with Disordered Steroidogenesis
Antley-Bixler Syndrome with Disordered Steroidogenesis 		6 0 2 0.17 0 0
CUI: C1960539
Disease: Aromatase deficiency
Aromatase deficiency 		6 0 2 0.17 0 0
CUI: C4021823
Disease: Ambiguous genitalia, male
Ambiguous genitalia, male 		13 0 3 0.17 0 0
CUI: C4022996
Disease: Abnormal sex determination
Abnormal sex determination 		15 0 3 0.15 0 0
CUI: C1955741
Disease: Glucocorticoid deficiency
Glucocorticoid deficiency 		8 0 2 0.14 0 0
CUI: C0345309
Disease: Hypoplasia of vagina
Hypoplasia of vagina 		17 0 3 0.14 0 0
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase 		17 0 3 0.14 0 0
CUI: C1848178
Disease: Female external genitalia in individual with 46,XY karyotype
Female external genitalia in individual with 46,XY karyotype 		17 0 3 0.14 0 0
CUI: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		9 0 2 0.13 0 0
CUI: C0342527
Disease: Deficiency of testosterone biosynthesis
Deficiency of testosterone biosynthesis 		18 0 3 0.13 0 0
CUI: C0016724
Disease: Froehlich's Syndrome
Froehlich's Syndrome 		1 0 1 0.12 0 0
CUI: C0021177
Disease: Increased Libido
Increased Libido 		1 0 1 0.12 0 0
CUI: C0154695
Disease: Diplegic Infantile Cerebral Palsy
Diplegic Infantile Cerebral Palsy 		1 0 1 0.12 0 0
CUI: C0154697
Disease: Cerebral Palsy, Quadriplegic, Infantile
Cerebral Palsy, Quadriplegic, Infantile 		1 0 1 0.12 0 0