MeSH Browser

MeSH Supplementary: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Unique ID: C565977
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565977
Registry Numbers: 0
Heading Mapped to: *Hyperandrogenism
Frequency: 0
Note: mutation in CYP21A2
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency MeSH Supplementary Concept Data 2025