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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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myopia

Schurrs-Hoeijmakers Syndrome

Joint Laxity, Short Stature, and Myopia

Myopia 1, X-linked, Nonsyndromal

Myopia 25, Autosomal Dominant, Nonsyndromic

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The gene product of P4HA2 when defective results in accumulation of collagen monomers resulting in abnormal eye growth.

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

Spastic Paraplegia with Psychomotor Retardation and Seizures

Singleton-Merten Syndrome 1

Kaufman Oculocerebrofacial Syndrome

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Temtamy Syndrome

Retinal Cone Dystrophy 3B

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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