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Concept information

Preferred term

Adrenal Hyperplasia, Congenital  

Type

  • mesh:Descriptor

Definition

  • A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.

Entry terms

  • Congenital Adrenal Hyperplasia
  • Hyperplasia, Congenital Adrenal

In other languages

URI

http://data.loterre.fr/ark:/67375/JVR-K9191K7D-V

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