MeSH Browser

MeSH Supplementary: Retinal Cone Dystrophy 3B
Unique ID: C563678
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563678
Entry Term(s): Cone Dystrophy with Night Blindness and Supernormal Rod Responses, KCNV2-Related
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 13
Note: mutation in KCNV2
Date of Entry: 2012/11/05

Retinal Cone Dystrophy 3B MeSH Supplementary Concept Data 2024