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Cortisone reductase deficiency MeSH Supplementary Concept Data 2022


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 Number
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 Preferred
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