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: C1955743
Disease: Mineralocorticoid deficiency
Mineralocorticoid deficiency
6 0 4 0.20 0 0
CUI: C0342541
Disease: Precocious pubarche
Precocious pubarche
30 0 7 0.17 0 0
CUI: C0266275
Disease: Ectopic adrenal gland
Ectopic adrenal gland
3 0 3 0.17 0 0
CUI: C4022554
Disease: Hyperpigmented genitalia
Hyperpigmented genitalia
3 0 3 0.17 0 0
Deficiency of testosterone biosynthesis
18 0 5 0.16 0 0
CUI: C4022695
Disease: Abnormality of the labia majora
Abnormality of the labia majora
4 0 3 0.16 0 0
Classic Congenital Adrenal Hyperplasia
4 0 3 0.16 0 0
CUI: C4021740
Disease: Increased circulating ACTH level
Increased circulating ACTH level
12 0 4 0.15 0 0
CUI: C4021124
Disease: Adrenocorticotropic hormone excess
Adrenocorticotropic hormone excess
5 0 3 0.15 0 0
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome
16 0 4 0.13 0 0
CUI: C1955741
Disease: Glucocorticoid deficiency
Glucocorticoid deficiency
8 0 3 0.13 0 0
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism
18 0 4 0.12 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency
10 0 3 0.12 0 0
CUI: C4025891
Disease: Ambiguous genitalia, female
Ambiguous genitalia, female
10 0 3 0.12 0 0
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
11 0 3 0.12 0 0
CUI: C4025888
Disease: Abnormality of the menstrual cycle
Abnormality of the menstrual cycle
11 0 3 0.12 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
22 0 4 0.11 0 0
Familial Glucocorticoid Deficiency Type 1
12 0 3 0.11 0 0
CUI: C4284917
Disease: Adrenal Gland Hyperplasia II
Adrenal Gland Hyperplasia II
2 0 2 0.11 0 0
CUI: C4285817
Disease: Cortisol deficiency
Cortisol deficiency
2 0 2 0.11 0 0
CUI: C1621895
Disease: Adrenal hyperplasia
Adrenal hyperplasia
33 0 5 0.11 0 0
Decreased circulating cortisol level
23 0 4 0.11 0 0
Inappropriate ACTH Secretion Syndrome
3 0 2 0.11 0 0
CUI: C0795855
Disease: Ring chromosome 15 syndrome
Ring chromosome 15 syndrome
3 0 2 0.11 0 0
CUI: C1970109
Disease: AROMATASE EXCESS SYNDROME
AROMATASE EXCESS SYNDROME
14 0 3 0.10 0 0