MeSH Browser

MeSH Supplementary: Foveal Hypoplasia, Isolated
Unique ID: C565005
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565005
Registry Numbers: 0
Heading Mapped to: Fovea Centralis / abnormalities; *Eye Diseases, Hereditary; *Nystagmus, Congenital
Frequency: 25
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Foveal Hypoplasia, Isolated MeSH Supplementary Concept Data 2025