MeSH Browser

MeSH Supplementary: Retinal cone dystrophy 2
Unique ID: C538363
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538363
Entry Term(s): Cone degeneration, autosomal dominant progressive; Cone-Rod Dystrophy 6
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 7
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Retinal cone dystrophy 2 MeSH Supplementary Concept Data 2024