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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[…][whonamedit.com]

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