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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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dysphagia

Cerebral Palsy, Spastic Quadriplegic, 3

Spinocerebellar Ataxia 42

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The abnormal gene product of mutated CACNA1G impacts firing patterns in neurons and other cells resulting in widespread CNS malfunction.

Spastic Paraplegia 11

3-methylglutaconic Aciduria with Cataracts, Neurologic Involvement and Neurtropenia

Cerebral Atrophy, Autosomal Recessive

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Optic Atrophy, Areflexia, Ataxia, Hearing Loss

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Myasthenic Syndromes, Congenital, Including AChR Deficiency

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CHARGE Syndrome

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Spinocerebellar Ataxia 1

Oculopharyngodistal Myopathy

Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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