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Up to: Hereditary disease, non-human animal · Syndromic disease, non-human animal
Abnormal gait, retinal dysplasia, cataracts, RORB-related, rabbit
Abnormal locomotion defined by the loss of typical jumping and blindness at birth due to retinal dysplasia and early-onset cataracts that occurs in rabbits due to a mutation in the RORB gene.
This condition has no sub-types.