Hypoadrenocorticism, Familial
"Hypoadrenocorticism, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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
| Descriptor ID |
D000075262
|
| MeSH Number(s) |
C19.053.500.263.500
|
| Concept/Terms |
Hypoadrenocorticism, Familial- Hypoadrenocorticism, Familial
- Familial Hypoadrenocorticism
- Familial Hypoadrenocorticisms
- Hypoadrenocorticisms, Familial
X-linked Adrenal Hypoplasia- X-linked Adrenal Hypoplasia
- Adrenal Hypoplasia, X-linked
- X linked Adrenal Hypoplasia
- Familial X-linked Addison Disease
- Familial X linked Addison Disease
- Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
- Addison Disease, X-Linked
- Addison Disease, X Linked
- X-Linked Addison Disease
- Cytomegalic Adrenocortical Hypoplasia
- Cytomegalic Adrenocortical Hypoplasias
- AHC with Isolated Gonadotropin Deficiency
- X-linked Congenital Adrenal Hypoplasia
- X linked Congenital Adrenal Hypoplasia
- Adrenal Hypoplasia, Congenital
- Congenital Adrenal Hypoplasia
- Congenital Adrenal Hypoplasias
- Hypoplasia, Congenital Adrenal
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