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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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albinism

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.

Albinism, Oculocutaneous, Type V

Albinism, Oculocutaneous, Type VII

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Hermansky-Pudlak Syndrome

Albinism, Oculocutaneous, Type I

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Eye in type IA oculocutaneous albinism

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Eye and lashes in type IA oculocutaneous albinism

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Fundus in type IA oculocutaneous albinism

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Hair in yellow mutant type oculocutaneous albinism

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Chédiak-Higashi Syndrome

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Albinism, Ocular Type 1

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Oculocerebral Syndrome with Hypopigmentation

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Oculocerebral syndrome with hypopigmentation in 3 individuals

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College of Medicine
Department of Ophthalmology and Vision Science
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