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Vitreoretinochoroidopathy MeSH Supplementary Concept Data 2022


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 Preferred
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Related
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