MeSH Browser

MeSH Supplementary: Retinal Cone Dystrophy 1
Unique ID: C566719
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566719
Entry Term(s): Cone Dystrophy, Autosomal Dominant; Retinal Cone Degeneration
Registry Numbers: 0
Heading Mapped to: *Retinal Degeneration; Retinal Cone Photoreceptor Cells / pathology
Frequency: 12
Note: aka RCD1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Retinal Cone Dystrophy 1 MeSH Supplementary Concept Data 2025