MeSH Browser

MeSH Supplementary: Night Blindness, Congenital Stationary, Autosomal Dominant 2
Unique ID: C566869
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566869
Entry Term(s): CSNBAD2; Night Blindness, Congenital Stationary, Rambusch Type
Heading Mapped to: *Night Blindness; *Eye Diseases, Hereditary
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Night Blindness, Congenital Stationary, Autosomal Dominant 2 MeSH Supplementary Concept Data 2024