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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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hypogonadism

Pseudohypoparathyroidism, Type 1A

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Congenital Disorder of Glycosylation, Type Ia

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Retinitis Pigmentosa, Deafness, Mental Retardation and Hypogonadism

Myotonic Dystrophy 2

Myotonic Dystrophy 1

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Iridescent lens opacities in a 52 yo patient with myotonic dystrophy

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Carpenter Syndrome

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External Ophthalmoplegia, POLG and mtDNA Mutations

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Bardet-Biedl Syndromes

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College of Medicine
Department of Ophthalmology and Vision Science
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