Disease: 21-hydroxylase deficiency ×
Source: ALL
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 AlteredExpression disease BEFREE Increased CYP2C19 activity could slightly ameliorate mineralocorticoid deficiency in 21OHD. 26970786 2016
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency 		0.020 Biomarker disease BEFREE CYP2C19 was genotyped in 21OHD patients with genotypes predicting severe congenital adrenal hyperplasia. 18957504 2009