OMIA:000869-9615 : Retinal dystrophy in Canis lupus familiaris (dog) |
In other species: domestic cat
Categories: Vision / eye phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 303100 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
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. (2010). OMIA:000869-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2011 | Robert, L., Sénéchal, A., Bocquet, B., Herbin, L., Chaudieu, G., Kalatzis, V., André, C., Hamel, C.P. : |
| Screening for a canine model of choroideremia exclusively identifies nonpathogenic CHM variants. Ophthalmic Res 45:155-63, 2011. Pubmed reference: 20861657. DOI: 10.1159/000313992. |
Edit History
- Created by Frank Nicholas on 02 Nov 2010