OMIA:000881-9615 : Retinal atrophy - Rod-cone dysplasia, CRX related in Canis lupus familiaris (dog)

In other species: domestic cat

Categories: Vision / eye phene

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 613829 (trait) , 602225 (gene)

Links to MONDO diseases:

Mendelian trait/disorder: unknown

Considered a defect: unknown

Species-specific description: Redundant - Information previously listed here about the canine cone transducin-gamma gene and cone degeneration has been moved to ' OMIA:002715-9615 : Cone degeneration in Canis lupus familiaris' [07/05/2023]

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:000881-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Edit History


  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Imke Tammen2 on 07 Jun 2023
  • Changed by Imke Tammen2 on 16 Oct 2023