OMIA:000519-9796 : Hypoadrenocorticism in Equus caballus (horse) |
In other species: dog , domestic cat , goat
Categories: Endocrine / exocrine gland phene (incl mammary gland)
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 240200 (trait) , 240300 (trait)
Mendelian trait/disorder: unknown
Disease-related: yes
Cross-species summary: Hypoadrenocorticism, or Addison’s disease, results from insufficient secretion of steroid hormones (glucocorticoids and mineralocorticoids) from the adrenal glands. In primary hypoadrenocorticism the disease is due to changes to the adrenal cortex, while secondary hypoadrenocorticism refers to deficiency of ACTH, produced in the pituitary gland. The disease can be further classified as typical (glucocorticoid and mineralocorticoid deficiency) with typical electrolyte changes or atypical (only glucocorticoid deficiency with no typical electrolyte changes). The atypical cases often progress to become typical.
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000519-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
1998 | Couetil, L.L., Hoffman, A.M. : |
Adrenal insufficiency in a neonatal foal Journal of the American Veterinary Medical Association 212:1594 ff., 1998. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005