OMIA:002317 : Abnormal gait, retinal dysplasia, cataracts, RORB-related

Categories: Behaviour / neurological phene

Possible human homologue (MIM number): 601972 (gene)

Links to MONDO diseases: No links.

Species in which this phene is found:
rabbit (Oryctolagus cuniculus)

Edit History


  • Created by Imke Tammen2 on 06 Apr 2021
  • Changed by Imke Tammen2 on 06 Apr 2021
  • Changed by Imke Tammen2 on 28 Oct 2022
  • Changed by Imke Tammen2 on 31 Oct 2022