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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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Baker-Gordon Syndrome

Schurrs-Hoeijmakers Syndrome

Epileptic Encephalopathy, Early Infantile 58

Mental Retardation, AD 31

Neurodevelopmental Disorder With or Without Seizures and Gait Abnormalities

Gabriele-de Vries Syndrome

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Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies

Congenital Heart Defects, Dysmorphic Facies, and Intellectual Developmental Disorder

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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.

Mental Retardation, X-Linked 99, Syndromic, Female-Restricted

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College of Medicine
Department of Ophthalmology and Vision Science
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