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Hereditary Ocular Disease: a Database of hereditary ocular disease.

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Keratosis Follicularis Spinulosa Decalvans, AD

Encephalocraniocutaneous Lipomatosis

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A defective FGFR1 gene product is unable to recognize the appropriate receptor in the cell surface and results in defective cell signaling.

Mandibulofacial Dysostosis with Alopecia

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Hypoparathyroidism, Familial Isolated

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GAPO Syndrome

IFAP (BRESHECK) Syndrome

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Hereditary Mucoepithelial Dysplasia

Ablepharon-Macrostomia Syndrome

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Oculodentodigital Dysplasia

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Keratosis Follicularis Spinulosa Decalvans, X-Linked

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Pagination

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College of Medicine
Department of Ophthalmology and Vision Science
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