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Adrenocortical Hypofunction, Chronic Primary Congenital MeSH Supplementary Concept Data 2025


MeSH Supplementary
Adrenocortical Hypofunction, Chronic Primary Congenital
Unique ID
C562711
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562711
Entry Term(s)
Addison Disease, Congenital
Registry Numbers
0
Heading Mapped to
*Adrenal Insufficiency
*Genetic Diseases, Inborn
Frequency
0
Date of Entry
2012/11/05
Revision Date
1955/01/01
Adrenocortical Hypofunction, Chronic Primary Congenital Preferred
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