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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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Hypotonia, Infantile, with Psychomotor Retardation And Characteristic Facies 2

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Retinitis Pigmentosa With or Without Skeletal Anomalies

Coloboma, Microphthalmia, Albinism, and Deafness

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Mutations in the MITF gene result in a defective transcription factor protein product that reduces the number of melanocytes thereby impacting multiple organ systems.

Meester-Loeys Syndrome

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ZTTK Syndrome

Cleft Palate, Psychomotor Retardation, and Distinctive Facial Features

Trichomegaly Plus Syndrome

GAPO Syndrome

Adrenoleukodystrophy, Autosomal

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Hallermann-Streiff Syndrome

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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