Hypoadrenocorticism, Familial [familiární hypoadrenokorticismus]
topical
- 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
Persistent link
https://www.medvik.cz/link/D000075262
Definition
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 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 0
- CO
- complications 0
- DI
- diagnosis 0
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 0
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 0
- GE
- genetics 0
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 0
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 0
- PP
- physiopathology 0
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 0
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records