OMIA:001222 : Leber congenital amaurosis |
Categories: Vision / eye phene
Possible human homologues (MIM numbers): 204100 (trait) , 180069 (gene) , 613794 (trait) , 618697 (trait)
Links to MONDO diseases: No links.
Cross-species summary: This disorder has been renamed in OMIA on the basis of the review by Miyadera et al. (2012). It is also known as retinal pigment epithelial dystrophy.
Species in which this phene is found:
dog (Canis lupus familiaris)
domestic cat (Felis catus)
Edit History
- Created by Frank Nicholas on 03 May 2005
- Changed by Frank Nicholas on 07 Dec 2011
- Changed by Frank Nicholas on 08 Dec 2011
- Changed by Frank Nicholas on 11 Jul 2012
- Changed by Frank Nicholas on 03 Sep 2012
- Changed by Frank Nicholas on 09 Dec 2017
- Changed by Frank Nicholas on 05 Jun 2019
- Changed by Imke Tammen2 on 25 Sep 2021