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OMIA:001613-9685 : Retinal dystrophy, early onset, Bengal in Felis catus (domestic cat)

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

Breed: Bengal (Cat) (VBO_0100040).
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

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2013). OMIA:001613-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

2011 Narfström, K., Menotti Raymond, M., Seeliger, M. :
Characterization of feline hereditary retinal dystrophies using clinical, functional, structural and molecular genetic studies. Vet Ophthalmol 14 Suppl 1:30-6, 2011. Pubmed reference: 21923821. DOI: 10.1111/j.1463-5224.2011.00915.x.

Edit History


  • Created by Frank Nicholas on 30 Sep 2011
  • Changed by Frank Nicholas on 16 Jan 2012
  • Changed by Frank Nicholas on 31 Jan 2013