MeSH Browser

MeSH Supplementary: Adrenal hyperplasia, congenital, type 5
Unique ID: C538237
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538237
Entry Term(s): 17-alpha-hydroxylase deficiency; Adrenal Hyperplasia V; Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase Deficiency; Adrenal hyperplasia, congenital due to 17-alpha-hydroxylase deficiency
Registry Numbers: 0
Heading Mapped to: *Adrenal Hyperplasia, Congenital
Frequency: 12
Date of Entry: 2010/06/25
Revision Date: 2012/08/24

Adrenal hyperplasia, congenital, type 5 MeSH Supplementary Concept Data 2025