DISEASES

Disease-gene associations mined from literature

Human genes for neovascular inflammatory vitreoretinopathy

Neovascular inflammatory vitreoretinopathy [DOID:9719]

A retinal and vitreous disease characterized by ocular inflammation, vascular dropout, large spots of hyperpigmentation, neovascularization of the peripheral and posterior retina, vitreous hemorrhage, and retinal detachment that has_material_basis_in heterozygous mutation in CAPN5 on chromosome 11q13.5.

Synonyms:  neovascular inflammatory vitreoretinopathy,  DOID:9719,  neovascular inflammatory vitreoretinopathies,  ADNIV,  autosomal dominant neovascular inflammatory vitreoretinopathy ...

Linkouts:  OMIM