Structured Summary
Abstract
Genetic or familial occurrence of ADDISONS DISEASE characterized by insufficient production of cortisol, aldosterone, and/or other hormones made in the adrenal cortex.
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Classification
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Synonyms
23 entry terms
- Hypoadrenocorticism, Familial
- Familial Hypoadrenocorticisms
- Hypoadrenocorticisms, Familial
- 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
- Addison Disease, X Linked
- Adrenal Hypoplasia, X-linked
- Congenital Adrenal Hypoplasia
- Congenital Adrenal Hypoplasias
- Cytomegalic Adrenocortical Hypoplasias
- Familial X linked Addison Disease
- Hypoplasia, Congenital Adrenal
- X linked Adrenal Hypoplasia
- X linked Congenital Adrenal Hypoplasia
- X-Linked Addison Disease
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2018(2010)
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AMA Style
References
- National Library of Medicine. Familial Hypoadrenocorticism. Medical Subject Headings (MeSH). 2026. Unique ID D000075262. http://id.nlm.nih.gov/mesh/2026/D000075262
- Familial Hypoadrenocorticism. In: Wikidata. https://www.wikidata.org/wiki/Q113372123