Familial Exudative Vitreoretinopathies D000080345

Related MeSH Hierarchy (5)

Diseases [C] » Eye Diseases [C11] » Eye Abnormalities » Familial Exudative Vitreoretinopathies

Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Familial Exudative Vitreoretinopathies

Diseases [C] » Eye Diseases [C11] » Retinal Diseases » Familial Exudative Vitreoretinopathies

Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Eye Abnormalities » Familial Exudative Vitreoretinopathies

Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Familial Exudative Vitreoretinopathies

Description

A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene.   MeSH

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