Vitreoretinochoroidopathy [Supplementary Concept]
mutation on BEST1 protein, human
Date introduced: August 25, 2010
MeSH Unique ID: C536352
Heading Mapped to:
Entry Terms:
- Autosomal dominant Vitreoretinochoroidopathy
- Vitreoretinochoroidopathy With Microcornea, Glaucoma, And Cataract
- Vitreoretinochoroidopathy dominant
- Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos
- ADVIRC
- Vitreoretinochoroidopathy, Autosomal Dominant
- Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma