Hypoadrenocorticism, Familial [familiární hypoadrenokorticismus]
- Terms
-
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 Browser
- CUI
- M000630038
- History note
- 2018(2010)
- Public note
- 2018; HYPOADRENOCORTICISM, FAMILIAL was indexed under ADRENAL INSUFFICIENCY 2010-2017
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology