MeSH Browser

MeSH Supplementary: Cortisone reductase deficiency
Unique ID: C536447
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536447
Entry Term(s): 11-beta-hydroxysteroid dehydrogenase, type i, deficiency of
Registry Numbers: 0
Heading Mapped to: Hirsutism / congenital; 11-beta-Hydroxysteroid Dehydrogenases / deficiency; *Steroid Metabolism, Inborn Errors; *46, XX Disorders of Sex Development
Frequency: 7
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Cortisone reductase deficiency MeSH Supplementary Concept Data 2025