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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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anemia

Coats Plus Syndrome

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Premature telomere shortening results from mutations in the gene CTC1 which allows chromosomes to degrade prematurely and shorten the time of cell divisions.

Hoyeraal-Hreidarsson Syndrome

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Révész Syndrome

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Pearson Marrow-Pancreas Syndrome

Wolfram Syndrome 2

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Wolfram Syndrome 1

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Gaucher Disease

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LCAT Deficiency

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College of Medicine
Department of Ophthalmology and Vision Science
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