NLM Logo

Adrenal Hyperplasia, Congenital MeSH Descriptor Data 2024


MeSH Heading
Adrenal Hyperplasia, Congenital
Tree Number(s)
C12.050.351.875.253.090.500
C12.200.706.316.090.500
C12.800.316.090.500
C16.131.939.316.129.500
C16.320.033
C16.320.565.925.249
C18.452.648.925.249
C19.053.440
C19.391.119.090.500
Unique ID
D000312
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000312
Scope Note
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 Version
ADRENAL HYPERPLASIA CONGEN
Entry Term(s)
Congenital Adrenal Hyperplasia
Hyperplasia, Congenital Adrenal
NLM Classification #
WK 700
See Also
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
Puberty, Precocious
Steroid 11-beta-Hydroxylase
Steroid 17-alpha-Hydroxylase
Steroid 21-Hydroxylase
Virilism
Public MeSH Note
80; was ADRENOGENITAL SYNDROME 1963-79
Online Note
use ADRENAL HYPERPLASIA, CONGENITAL to search ADRENOGENITAL SYNDROME 1966-79
History Note
80; was ADRENOGENITAL SYNDROME 1963-79
Date Established
1980/01/01
Date of Entry
1999/01/01
Revision Date
2021/06/30
Adrenal Hyperplasia, Congenital Preferred
page delivered in 0.25s