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
database cross reference
- OMIM:193235 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:H35.2 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- ICD-10:H35.2 (Attributed (The ICD10 code is attributed by Orphanet))
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some <1 / 1 000 000
- present_in some Worldwide and has_cases/families_value value 99.0
- has_inheritance some autosomal dominant
- part_of some Isolated vitreoretinopathy
- part_of some Rare retinal vasculopathy
- part_of some Rare genetic retinal vasculopathy
- has_age_of_onset some all ages
Related from: