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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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corneal opacities

Corneal Dystrophy, Posterior Polymorphous 4

Galloway-Mowat Syndrome

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Familial Exudative Vitreoretinopathy, EVR5

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Retinal Nonattachment, Congenital

Cataracts, CRYAA Mutations

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Microphthalmia, Syndromic 7

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Oculoauricular Syndrome

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Neuraminidase Deficiency

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Tyrosinemia, Type II

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Corneal opacities in tyrosinemia

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Sjogren-Larsson Syndrome

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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