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: C2751825
Disease: PREMATURE OVARIAN FAILURE 7 (disorder)
PREMATURE OVARIAN FAILURE 7 (disorder) 		1 9 1 0.33 5 0.21
CUI: C3151406
Disease: SPERMATOGENIC FAILURE 8
SPERMATOGENIC FAILURE 8 		1 0 1 0.33 0 0
CUI: C3502132
Disease: Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal
Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal 		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: C3805515
Disease: Microorchidism
Microorchidism 		1 0 1 0.33 0 0
CUI: C4022708
Disease: Midshaft hypospadias
Midshaft hypospadias 		1 0 1 0.33 0 0
CUI: C4022829
Disease: Abnormal urine potassium concentration
Abnormal urine potassium concentration 		1 0 1 0.33 0 0
CUI: C4024645
Disease: Incomplete male pseudohermaphroditism
Incomplete male pseudohermaphroditism 		1 0 1 0.33 0 0
CUI: C4024842
Disease: Generalized bronze hyperpigmentation
Generalized bronze hyperpigmentation 		1 0 1 0.33 0 0
CUI: C4479664
Disease: ADRENAL INSUFFICIENCY, NR5A1-RELATED
ADRENAL INSUFFICIENCY, NR5A1-RELATED 		1 2 1 0.33 1 4.8E-02
CUI: C4707238
Disease: Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency 		1 0 1 0.33 0 0
CUI: C0403810
Disease: Oligosynaptic Infertility
Oligosynaptic Infertility 		2 3 1 0.25 2 9.5E-02
CUI: C0949331
Disease: Gonadal Agenesis
Gonadal Agenesis 		2 0 1 0.25 0 0
CUI: C2118097
Disease: Agonadism
Agonadism 		2 0 1 0.25 0 0
CUI: C3151055
Disease: ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE
ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE 		2 0 1 0.25 0 0
CUI: C4024734
Disease: Low maternal serum estriol
Low maternal serum estriol 		2 0 1 0.25 0 0
CUI: C4025253
Disease: Streaky metaphyseal sclerosis
Streaky metaphyseal sclerosis 		2 0 1 0.25 0 0
CUI: C4072894
Disease: Decreased circulating androgen level
Decreased circulating androgen level 		2 0 1 0.25 0 0
CUI: C4331349
Disease: Steroidogenic Acute Regulatory Protein Deficiency
Steroidogenic Acute Regulatory Protein Deficiency 		2 0 1 0.25 0 0
CUI: C4284088
Disease: MIRAGE SYNDROME
MIRAGE SYNDROME 		8 0 2 0.22 0 0
CUI: C0271750
Disease: Adrenal calcification
Adrenal calcification 		3 0 1 0.20 0 0
CUI: C0452147
Disease: Hypospadias, penoscrotal
Hypospadias, penoscrotal 		9 0 2 0.20 0 0
CUI: C0860158
Disease: Leydig Cell Hypoplasia
Leydig Cell Hypoplasia 		3 0 1 0.20 0 0
CUI: C1261504
Disease: Congenital absence of both testes
Congenital absence of both testes 		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