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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency : ウィキペディア英語版
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OH CAH), in all its forms, accounts for over 95% of diagnosed cases of congenital adrenal hyperplasia, and "CAH" in most contexts refers to 21-hydroxylase deficiency. An overview of the other types of CAH is presented in the main article.
==Degree of severity==
The condition can be classified into "salt-wasting", "simple virilizing", and "non-classical" forms.
The salt-wasting and simple virilizing types are sometimes grouped together as "classical".

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