OMIA:000508-319699 : Hyperparathyroidism in Equus asinus x caballus (mule) |
In other species: dog , domestic cat , horse
Categories: Endocrine / exocrine gland phene (incl mammary gland)
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 145000 (trait) , 145001 (trait) , 239199 (trait) , 239200 (trait) , 256120 (trait) , 600166 (trait)
Links to MONDO diseases:
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Hyperfunction of the parathyroid glands resulting in the overproduction of parathyroid hormone. It may be primary or secondary; primary hyperparathyroidism is caused by parathyroid adenoma, parathyroid hyperplasia, parathyroid carcinoma, and multiple endocrine neoplasia. It is associated with hypercalcemia and hypophosphatemia. ... Secondary hyperparathyroidism is caused by the chronic stimulation of the parathyroid glands in patients with chronic renal failure, rickets, and malabsorption syndromes. [NCIT:C48259]
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:000508-319699: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2023 | Townsend, K.S., Johnson, P.J., Donnelly, L.L., LaCarrubba, A.M., Lattimer, J.C., Havis, B., Springer, N.L., Kim, D.Y. : |
| Concurrent chronic lymphocytic leukemia and primary hyperparathyroidism in a mule. J Vet Intern Med , 2023. Pubmed reference: 37118906. DOI: 10.1111/jvim.16714. |
Edit History
- Created by Imke Tammen2 on 01 May 2023