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: C3502132
Disease: Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal
Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal 		1 0 1 0.25 0 0
CUI: C4022708
Disease: Midshaft hypospadias
Midshaft hypospadias 		1 0 1 0.25 0 0
CUI: C4022829
Disease: Abnormal urine potassium concentration
Abnormal urine potassium concentration 		1 0 1 0.25 0 0
CUI: C4024842
Disease: Generalized bronze hyperpigmentation
Generalized bronze hyperpigmentation 		1 0 1 0.25 0 0
CUI: C4707238
Disease: Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency 		1 0 1 0.25 0 0
CUI: C4746851
Disease: PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1
PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1 		1 0 1 0.25 0 0
CUI: C0014536
Disease: Epidural Neoplasms
Epidural Neoplasms 		2 0 1 0.20 0 0
CUI: C0342387
Disease: LH - luteinizing hormone deficiency
LH - luteinizing hormone deficiency 		2 0 1 0.20 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 0.20 0 0
CUI: C4024734
Disease: Low maternal serum estriol
Low maternal serum estriol 		2 0 1 0.20 0 0
CUI: C4072894
Disease: Decreased circulating androgen level
Decreased circulating androgen level 		2 0 1 0.20 0 0
CUI: C4331349
Disease: Steroidogenic Acute Regulatory Protein Deficiency
Steroidogenic Acute Regulatory Protein Deficiency 		2 0 1 0.20 0 0
CUI: C0016399
Disease: Epilepsy, Partial, Motor
Epilepsy, Partial, Motor 		3 0 1 0.17 0 0
CUI: C0271750
Disease: Adrenal calcification
Adrenal calcification 		3 0 1 0.17 0 0
CUI: C3489793
Disease: 46,XY Sex Reversal 3
46,XY Sex Reversal 3 		3 0 1 0.17 0 0
CUI: C3502131
Disease: Adrenal Insufficiency, Congenital
Adrenal Insufficiency, Congenital 		3 0 1 0.17 0 0
CUI: C4021573
Disease: Patchy hypo- and hyperpigmentation
Patchy hypo- and hyperpigmentation 		3 0 1 0.17 0 0
CUI: C4024615
Disease: Adipose tissue loss
Adipose tissue loss 		3 0 1 0.17 0 0
CUI: C0152444
Disease: Hydrorhachis
Hydrorhachis 		4 0 1 0.14 0 0
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		4 0 1 0.14 0 0
CUI: C1168239
Disease: Asymmetry of the ears
Asymmetry of the ears 		4 0 1 0.14 0 0
CUI: C1850568
Disease: Nakajo syndrome
Nakajo syndrome 		4 0 1 0.14 0 0
CUI: C0239598
Disease: Swelling of finger
Swelling of finger 		5 0 1 0.12 0 0
CUI: C0342474
Disease: Lipoid congenital adrenal hyperplasia
Lipoid congenital adrenal hyperplasia 		5 0 1 0.12 0 0
CUI: C0520933
Disease: Abnormal spermatogenesis
Abnormal spermatogenesis 		5 0 1 0.12 0 0