Exudative retinopathy familial, autosomal dominant: A rare progressive eye disorder which is inherited in a dominant manner. The development of the retinal blood vessels is incomplete resulting in parts of the retina having no blood vessels which is necessary for it's function. The disorder is caused by a genetic defect on chromosome 11q14-q21 and the severity of the condition is variable. More detailed information about the symptoms, causes, and treatments of Exudative retinopathy familial, autosomal dominant is available below.
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