OMIA:000866-9541 : Retinal degeneration in Macaca fascicularis (crab-eating macaque)

In other species: domestic cat , horse , taurine cattle

Categories: Vision / eye phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

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. (2019). OMIA:000866-9541: Online Mendelian Inheritance in Animals (OMIA) [dataset].


2018 Ikeda, Y., Nishiguchi, K.M., Miya, F., Shimozawa, N., Funatsu, J., Nakatake, S., Fujiwara, K., Tachibana, T., Murakami, Y., Hisatomi, T., Yoshida, S., Yasutomi, Y., Tsunoda, T., Nakazawa, T., Ishibashi, T., Sonoda, K.H. :
Discovery of a Cynomolgus Monkey Family With Retinitis Pigmentosa. Invest Ophthalmol Vis Sci 59:826-830, 2018. Pubmed reference: 29411010. DOI: 10.1167/iovs.17-22958.

Edit History

  • Created by Frank Nicholas on 22 Oct 2019