MeSH Browser

MeSH Supplementary: Retinoschisis of Fovea
Unique ID: C538369
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538369
Entry Term(s): Familial foveal retinoschisis; Foveal retinoschisis
Registry Numbers: 0
Heading Mapped to: *Retinoschisis
Frequency: 26
Note: A hereditary austosomal recessive form of retinoschisis affecting the FOVEA CENTRALIS and characterized by mild visual loss, bilateral foveal dystrophy, and abnormal electroretinogram findings. OMIM: 268080
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Retinoschisis of Fovea MeSH Supplementary Concept Data 2025