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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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encephalopathy

Hypotonia, Infantile, with Psychomotor Retardation And Characteristic Facies 2

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Encephalopathy, Progressive, Early-Onset, wtih Brain Atrophy and Spasticity

PEHO-Like Syndrome

Epileptic Encephalopathy, Early Infantile 47

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Mutations in the FGF12 gene, whose product is one of the fibroblast growth factor family, has widespread impacts in the eye and CNS.

Mitochondrial DNA Depletion Syndrome 3

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Optic Atrophy, Areflexia, Ataxia, Hearing Loss

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Congenital Disorder of Glycosylation, Type Ia

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MELAS Syndrome

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College of Medicine
Department of Ophthalmology and Vision Science
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