21-ohd - a classic form of congenital adrenal hyperplasia that is characterized by severe 21-hydroxylase deficiency, resulting in glucocorticoid and mineralocorticoid deficiency, without clinically significant salt wasting, and androgen excess, which causes virilization in female infants.
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Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on 21-ohd for any updates.