MeSH Browser

MeSH Supplementary: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Unique ID: C566474
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566474
Entry Term(s): CSNBAD1; Night Blindness, Congenital Stationary, Rhodopsin-Related
Registry Numbers: 0
Heading Mapped to: *Night Blindness; *Eye Diseases, Hereditary
Frequency: 0
Note: mutation in rhodopsin
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Night Blindness, Congenital Stationary, Autosomal Dominant 1 MeSH Supplementary Concept Data 2025