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ENAdrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency (AH3)
Alias:
21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, Due to 21-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia 1
Cah1
Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia
Cyp21 Deficiency
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hyperandrogenism Nonclassic Type Due to 21-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Deficiency
Virilizing Adrenal Hyperplasia
Adrenal Hyperplasia Type Iii
21 Hydroxylase Deficiency
Adrenal Hyperplasia Iii
Adrenal Hyperplasia 3
21-Ohd Cah
Ah-Iii
Ah3
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Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency, also known as 21-hydroxylase deficiency, is related to classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency and lipoid congenital adrenal hyperplasia. An important gene associated with Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency is CYP21A2 (Cytochrome P450 Family 21 Subfamily A Member 2). The drugs Hydrocortisone-17-butyrate and Dexamethasone have been mentioned in the context of this disorder. Affiliated tissues include adrenal cortex and testes, and related phenotypes are hypertension and fever
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