MeSH Browser

MeSH Supplementary: Vitreoretinochoroidopathy
Unique ID: C536352
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536352
Entry Term(s): ADVIRC; Autosomal dominant Vitreoretinochoroidopathy; Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma; Vitreoretinochoroidopathy With Microcornea, Glaucoma, And Cataract; Vitreoretinochoroidopathy dominant; Vitreoretinochoroidopathy, Autosomal Dominant; Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos
Registry Number: 0
Heading Mapped to: *Retinal Degeneration; *Eye Diseases, Hereditary; *Choroid Diseases
Frequency: 17
Note: mutation on BEST1 protein, human
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Vitreoretinochoroidopathy MeSH Supplementary Concept Data 2024