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: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism 		18 0 5 0.20 0 0
CUI: C3838731
Disease: Familial hyperaldosteronism type 1
Familial hyperaldosteronism type 1 		6 0 3 0.20 0 0
CUI: C3713420
Disease: Familial Hyperaldosteronism
Familial Hyperaldosteronism 		15 0 4 0.17 0 0
CUI: C4304832
Disease: Primary pigmented nodular adrenocortical disease
Primary pigmented nodular adrenocortical disease 		22 0 5 0.17 0 0
CUI: C0042420
Disease: Vasovagal syncope
Vasovagal syncope 		16 0 4 0.17 0 0
CUI: C3838758
Disease: Familial hyperaldosteronism type 3
Familial hyperaldosteronism type 3 		2 0 2 0.17 0 0
CUI: C3887949
Disease: Apparent mineralocorticoid excess
Apparent mineralocorticoid excess 		23 0 5 0.17 0 0
CUI: C3669121
Disease: 11-Beta-hydroxylase deficiency
11-Beta-hydroxylase deficiency 		10 0 3 0.16 0 0
CUI: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia 		25 0 5 0.16 0 0
CUI: C0271862
Disease: Idiopathic parathyroidism
Idiopathic parathyroidism 		3 0 2 0.15 0 0
CUI: C0302840
Disease: Toxic thyroid adenoma
Toxic thyroid adenoma 		3 0 2 0.15 0 0
CUI: C0597853
Disease: high renin hypertension
high renin hypertension 		3 0 2 0.15 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 3 0.15 0 0
CUI: C0268292
Disease: Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency 		11 0 3 0.15 0 0
CUI: C4025651
Disease: Increased circulating cortisol level
Increased circulating cortisol level 		11 0 3 0.15 0 0
CUI: C0027577
Disease: Nelson Syndrome
Nelson Syndrome 		4 0 2 0.14 0 0
CUI: C0151620
Disease: Hypertensive Encephalopathy
Hypertensive Encephalopathy 		4 0 2 0.14 0 0
CUI: C0264641
Disease: Endocrine hypertension
Endocrine hypertension 		4 0 2 0.14 0 0
CUI: C0271725
Disease: Iatrogenic Cushing's disease
Iatrogenic Cushing's disease 		4 0 2 0.14 0 0
CUI: C0334041
Disease: Osteoma cutis
Osteoma cutis 		4 0 2 0.14 0 0
CUI: C0342549
Disease: Familial Testotoxicosis
Familial Testotoxicosis 		20 0 4 0.14 0 0
CUI: C1300206
Disease: Blomstrand dysplasia
Blomstrand dysplasia 		4 0 2 0.14 0 0
CUI: C2678367
Disease: Renal Tubular Dysgenesis With Choanal Atresia And Athelia
Renal Tubular Dysgenesis With Choanal Atresia And Athelia 		4 0 2 0.14 0 0
CUI: C2932716
Disease: Pseudohypoparathyroidism Type 1C
Pseudohypoparathyroidism Type 1C 		4 0 2 0.14 0 0
CUI: C4014803
Disease: ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2
ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2 		4 0 2 0.14 0 0