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Retinal Cone Dystrophy 1 MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Retinal Degeneration
Retinal Cone Photoreceptor Cells / *pathology
Frequency
11
Note
aka RCD1
Date of Entry
2012/11/05
Revision Date
2013/11/06
Retinal Cone Dystrophy 1 Preferred
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