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Hypoadrenocorticism, Familial MeSH Descriptor Data 2023


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
Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200
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
2017/07/11
Revision Date
2017/06/20
Hypoadrenocorticism, Familial Preferred
Complex Glycerol Kinase Deficiency Narrower
Xp21 Contiguous Gene Deletion Syndrome Broader
X-linked Adrenal Hypoplasia Narrower
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