Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
0.020 Biomarker disease BEFREE Carriers of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) demonstrate increased secretion of cortisol precursors following ACTH stimulation, suggestive of impaired cortisol production and compensatory increases in hypothalamic corticotropin-releasing hormone (CRH) secretion. 28500827 2017
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
0.020 AlteredExpression disease BEFREE Levels of corticotropin-releasing hormone are elevated in patients with depression and anxiety and are expected to be elevated in patients with congenital adrenal hyperplasia; it is unknown whether patients with 21-hydroxylase deficiency have an increased incidence of these psychiatric disorders. 11848730 2002