Autosomal dominant neovascular inflammatory vitreoretinopathy

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A rare, genetic, vitreoretinal degeneration characterized by a slowly progressive vitreoretinopathy with onset during the second or third decade of life. The disease initially presents as autoimmune uveitis with reduction in the b-wave on electroretinography, and progresses with development of photoreceptor degeneration, vitreous hemorrhage, cystoid macular edema, retinal neovascularization, intraocular fibrosis, secondary glaucoma, and retinal detachment leading to phthisis and complete blindness.

Synonyms: ADNIV

This is just here as a test because I lose it

Term information

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OMIM:193235

ICD-10:H35.2

notation

ORPHA:329211