OMIA:001670-9615 : Rod dysplasia in Canis lupus familiaris (dog)
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
Cross-species summary: This disorder has been renamed in OMIA on the basis of the review by Miyadera et al. (2012)
Species-specific symbol: rd
Have human generated variants been created, e.g. through genetic engineering and gene editing
Norwegian Elkhound (Dog) (VBO_0200955).
Breeds in which the phene has been documented. For breeds in which a likely causal variant has been documented, see the variant table below
Cite this entry
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.
|2012||Miyadera, K., Acland, G.M., Aguirre, G.D. :|
|Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies. Mamm Genome 23:40-61, 2012. Pubmed reference: 22065099. DOI: 10.1007/s00335-011-9361-3.|
|1978||Aguirre, G. :|
|Retinal degenerations in the dog. I. Rod dysplasia. Exp Eye Res 26:233-53, 1978. Pubmed reference: 639877.|
- Created by Frank Nicholas on 02 Dec 2011