Adrenal Hyperplasia, Congenital D000312

Related MeSH Hierarchy (9)

Diseases [C] » Urogenital Diseases [C12] » Urogenital Abnormalities » Disorders of Sex Development » Adrenogenital Syndrome » Adrenal Hyperplasia, Congenital

Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Adrenal Hyperplasia, Congenital

Diseases [C] » Endocrine System Diseases [C19] » Adrenal Gland Diseases » Adrenal Hyperplasia, Congenital

Diseases [C] » Endocrine System Diseases [C19] » Gonadal Disorders » Disorders of Sex Development » Adrenogenital Syndrome » Adrenal Hyperplasia, Congenital

Description

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.   MeSH

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Phase 1 Indicated Drugs (2)

Other Experimental Indicated Drugs (1)


Organization Involved with Phase 4 Indications (2)

Organization Involved with Phase 3 Indications (3)

Organization Involved with Phase 1 Indications (3)

Organization Involved with Other Experimental Indications (2)

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