OMIA:001791-9685 : Intestinal cobalamin (vitamin B12) malabsorption, generic in Felis catus (domestic cat) |
In other species: dog
Categories: Homeostasis / metabolism phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 261100 (trait) , 618882 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: similar to: Imerslund-Gräsbeck syndrome (IGS1) (selective cobalamin malabsorption; megaloblastic anemia 1 (MGA1)) and Imerslund-Gräsbeck syndrome 2; IGS2
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. (2013). OMIA:001791-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 2023 | Siani, G., Mercaldo, B., Alterisio, M.C., Di Loria, A. : |
| Vitamin B12 in cats: nutrition, metabolism, and disease. Animals (Basel) 13, 2023. Pubmed reference: 37174511. DOI: 10.3390/ani13091474. | |
| 2012 | Watanabe, T., Hoshi, K., Zhang, C., Ishida, Y., Sakata, I. : |
| Hyperammonaemia due to cobalamin malabsorption in a cat with exocrine pancreatic insufficiency. J Feline Med Surg 14:942-5, 2012. Pubmed reference: 22907395. DOI: 10.1177/1098612X12458101. | |
| 2003 | Salvadori, C., Cantile, C., De, Ambrogi, G., Arispici, M. : |
| Degenerative myelopathy associated with cobalamin deficiency in a cat Journal of Veterinary Medicine - Series A 50:292-6, 2003. Pubmed reference: 12887621. | |
| 2001 | Ruaux, C.G., Steiner, J.M., Williams, D.A. : |
| Metabolism of amino acids in cats with severe cobalamin deficiency American Journal of Veterinary Research 62:1852-1858, 2001. Pubmed reference: 11763170. |
Edit History
- Created by Frank Nicholas on 23 Apr 2013