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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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microcephaly

Intellectual Disability with Dysmorphic Facies and Ptosis

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Optic Atrophy 11

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.

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

Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 2

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Mitochondrial DNA Depletion Syndrome 3

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Rubinstein-Taybi Syndrome 2

Cerebral Palsy, Spastic Quadriplegic, 3

Heart and Brain Malformation Syndrome

Hypotonia, Infantile, with Psychomotor Retardation And Characteristic Facies 1

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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