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: C0266432
Disease: Leydig cell agenesis
Leydig cell agenesis 		6 21 3 0.50 6 0.29
CUI: C0220761
Disease: Dizygotic twins (disorder)
Dizygotic twins (disorder) 		1 0 1 0.33 0 0
CUI: C0233200
Disease: Cullen's sign
Cullen's sign 		1 0 1 0.33 0 0
CUI: C1382398
Disease: Increased capillary permeability (finding)
Increased capillary permeability (finding) 		1 0 1 0.33 0 0
CUI: C2585739
Disease: Hyperreactio luteinalis
Hyperreactio luteinalis 		1 0 1 0.33 0 0
CUI: C3494162
Disease: Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous
Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous 		1 0 1 0.33 0 0
CUI: C3714042
Disease: 46,XY Disorder of Sex Development Due To LH Defects
46,XY Disorder of Sex Development Due To LH Defects 		1 0 1 0.33 0 0
CUI: C4024645
Disease: Incomplete male pseudohermaphroditism
Incomplete male pseudohermaphroditism 		1 0 1 0.33 0 0
CUI: C4521591
Disease: Peripheral precocious puberty
Peripheral precocious puberty 		5 0 2 0.33 0 0
CUI: C0473311
Disease: Hemorrhagic cyst of ovary
Hemorrhagic cyst of ovary 		2 0 1 0.25 0 0
CUI: C0085649
Disease: Peripheral edema
Peripheral edema 		3 0 1 0.20 0 0
CUI: C1960447
Disease: Hypergonadotropic amenorrhea
Hypergonadotropic amenorrhea 		3 0 1 0.20 0 0
CUI: C2673497
Disease: Leydig Cell Hypoplasia, Type II
Leydig Cell Hypoplasia, Type II 		3 0 1 0.20 0 0
CUI: C2674612
Disease: Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty
Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty 		3 1 1 0.20 1 0.17
CUI: C3489793
Disease: 46,XY Sex Reversal 3
46,XY Sex Reversal 3 		3 0 1 0.20 0 0
CUI: C3668935
Disease: Luteinizing Hormone Resistance, Female
Luteinizing Hormone Resistance, Female 		3 3 1 0.20 1 0.12
CUI: C4016252
Disease: LEYDIG HYPOPLASIA, TYPE I
LEYDIG HYPOPLASIA, TYPE I 		3 0 1 0.20 0 0
CUI: C4023702
Disease: Hyoplasia of the Leydig cells
Hyoplasia of the Leydig cells 		3 0 1 0.20 0 0
CUI: C0149952
Disease: Torsion of ovary
Torsion of ovary 		4 0 1 0.17 0 0
CUI: C0342549
Disease: Familial Testotoxicosis
Familial Testotoxicosis 		20 17 3 0.15 2 9.5E-02
CUI: C1859979
Disease: Precocious puberty in males
Precocious puberty in males 		5 0 1 0.14 0 0
CUI: C4072885
Disease: Increased serum testosterone level
Increased serum testosterone level 		5 0 1 0.14 0 0
CUI: C0018050
Disease: Gonadal Disorders
Gonadal Disorders 		6 0 1 0.12 0 0
CUI: C0342510
Disease: Ovarian dysgenesis
Ovarian dysgenesis 		6 0 1 0.12 0 0
CUI: C0023600
Disease: Leydig cell hyperplasia
Leydig cell hyperplasia 		7 2 1 0.11 2 0.33