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: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 10 44 0.45 5 0.50
CUI: C3887896
Disease: Primary Adrenal Insufficiency
Primary Adrenal Insufficiency 		27 2 11 0.16 1 0.17
CUI: C1836623
Disease: Decreased circulating cortisol level
Decreased circulating cortisol level 		23 0 10 0.15 0 0
CUI: C0857899
Disease: Decreased circulating aldosterone level
Decreased circulating aldosterone level 		16 0 9 0.15 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 17 0.14 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 13 19 0.13 1 5.9E-02
CUI: C0020625
Disease: Hyponatremia
Hyponatremia 		109 0 18 0.13 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		55 0 11 0.11 0 0
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 0 11 0.11 0 0
CUI: C2936858
Disease: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 		50 0 10 0.11 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting 		22 0 7 0.10 0 0
CUI: C0268287
Disease: Deficiency of steroid 21-monooxygenase
Deficiency of steroid 21-monooxygenase 		54 0 10 0.10 0 0
CUI: C1621895
Disease: Adrenal hyperplasia
Adrenal hyperplasia 		33 0 8 0.10 0 0
CUI: C4049650
Disease: Familial Glucocorticoid Deficiency Type 1
Familial Glucocorticoid Deficiency Type 1 		12 0 6 0.10 0 0
CUI: C0342388
Disease: Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency (disorder) 		24 0 7 0.10 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms 		94 0 13 9.8E-02 0 0
CUI: C0001622
Disease: Adrenal Gland Hyperfunction
Adrenal Gland Hyperfunction 		50 0 9 9.7E-02 0 0
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		16 0 6 9.7E-02 0 0
CUI: C1291314
Disease: Deficiency of monooxygenase
Deficiency of monooxygenase 		17 0 6 9.5E-02 0 0
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism 		18 0 6 9.4E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome 		42 0 8 9.3E-02 0 0
CUI: C0877056
Disease: Hypoglycemic seizures
Hypoglycemic seizures 		19 0 6 9.2E-02 0 0
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome 		126 0 15 9.2E-02 0 0
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia 		32 0 7 9.1E-02 0 0
CUI: C4284088
Disease: MIRAGE SYNDROME
MIRAGE SYNDROME 		8 0 5 9.1E-02 0 0