Related MeSH Hierarchy (5)
Diseases [C] » Eye Diseases [C11] » Eye Abnormalities » Retinal Dysplasia
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Retinal Dysplasia
Diseases [C] » Eye Diseases [C11] » Retinal Diseases » Retinal Dysplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Eye Abnormalities » Retinal Dysplasia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Retinal Dysplasia
Description
Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. MeSH
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