OMIA:001185-9685 : Retinoschisis in Felis catus (domestic cat) |
In other species: dog
Categories: Vision / eye phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 180270 (trait) , 268080 (trait) , 268100 (trait) , 312700 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: splitting of the retina into two layers; inherited, acquired and secondary forms have been reported
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:001185-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2023 | Di Bernardo, J., Newkirk, K., Hendrix, D. : |
| Retinoschisis: a retrospective study of an uncommon retinal change in cats and dogs. J Comp Pathol 207:30-32, 2023. Pubmed reference: 37925755. DOI: 10.1016/j.jcpa.2023.10.001. |
Edit History
- Created by Imke Tammen2 on 07 Nov 2023