Create issue ticket

1 Possible Causes for Caused by Mutation in the Retinol Dehydrogenase 12 Gene

  • Leber Congenital Amaurosis

    - A dictionary of medical eponyms Related people Theodor Karl Gustav von Leber Syndrome characterised by severe visual deficiency, with total or nearly total blindness, present at birth or shortly thereafter; pendular or searching nystagmus, sunken eyeballs, photophobia, and the digito-ocular sign[…][]

Further symptoms