Congenital adrenal hyperplasia (CAH) is an inherited endocrine disorder caused by a steroidogenic enzyme deficiency that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgyny manifestations, depending of the type and the severity of the disease.
Comprehensive, easy-to-understand information about this condition
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adrenocortical hypofunction, chronic primary congenital
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congenital lipoid adrenal hyperplasia due to STAR deficency
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congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency
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classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency
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congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
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