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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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dystonia

Dystonia, Childhood Onset, With Optic Atrophy

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Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy, Childhood-Onset

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.

Cataracts, Congenital, Intellectual Disability, Abnormal Striatum, and ADHD

Ataxia with Oculomotor Apraxia 4

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Spastic Ataxia 2

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Ataxia with Oculomotor Apraxia 2

Wilson Disease

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Neurodegeneration with Brain Iron Accumulation

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Pantothenate Kinase-Associated Neurodegeneration

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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