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

In other species: domestic cat

Categories: Vision / eye phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 613829 (trait) , 602225 (gene)

Links to relevant human diseases in MONDO:

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]

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:000881-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset].

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