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Hypoadrenocorticism, Familial MeSH Descriptor Data 2025


MeSH Heading
Hypoadrenocorticism, Familial
Tree Number(s)
C19.053.500.263.500
Unique ID
D000075262
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000075262
Scope Note
Genetic or familial occurrence of ADDISONS DISEASE characterized by insufficient production of cortisol, aldosterone, and/or other hormones made in the adrenal cortex.
Entry Term(s)
AHC with Isolated Gonadotropin Deficiency
Addison Disease, X-Linked
Adrenal Hypoplasia, Congenital
Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
Complex Glycerol Kinase Deficiency
Cytomegalic Adrenocortical Hypoplasia
Familial X-linked Addison Disease
X-linked Adrenal Hypoplasia
X-linked Congenital Adrenal Hypoplasia
Xp21 Contiguous Gene Deletion Syndrome
Public MeSH Note
2018; HYPOADRENOCORTICISM, FAMILIAL was indexed under ADRENAL INSUFFICIENCY 2010-2017
History Note
2018(2010)
Date Established
2018/01/01
Date of Entry
2024/08/09
Revision Date
2024/07/22
Hypoadrenocorticism, Familial Preferred
X-linked Adrenal Hypoplasia Narrower
Complex Glycerol Kinase Deficiency Narrower
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