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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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neurodegeneration

Encephalopathy, Progressive, with Amyotrophy and Optic Atrophy

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Mutations in the TBCE gene result in improper folding of beta-tubulin that is part of the microtubules located in the cytoskeleton.

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

Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation

Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency

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Adrenoleukodystrophy, X-Linked

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Sandhoff Disease

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Neuronal Ceroid Lipofuscinoses

Tay-Sachs Disease

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Niemann-Pick Disease, Types C1 (D)

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Niemann-Pick Disease, Types A and B

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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