Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency (AH3)

Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency(来自ICD-11)

别称:

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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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

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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