familiární hypoadrenokorticismus [Hypoadrenocorticism, Familial]
- Termíny
-
Addison Disease, X-Linked
Adrenal Hypoplasia, Congenital
Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism
AHC with Isolated Gonadotropin Deficiency
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
Genetic or familial occurrence of ADDISONS DISEASE characterized by insufficient production of cortisol, aldosterone, and/or other hormones made in the adrenal cortex.
- DUI
- D000075262 MeSH Prohlížeč
- CUI
- M000630038
- Historická pozn.
- 2018(2010)
- Veřejná pozn.
- 2018; HYPOADRENOCORTICISM, FAMILIAL was indexed under ADRENAL INSUFFICIENCY 2010-2017
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