MeSH Browser

MeSH Supplementary: Night Blindness, Congenital Stationary, Autosomal Dominant 3
Unique ID: C566475
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566475
Entry Term(s): CSNBAD3; Night Blindness, Congenital Stationary, Nougaret Type
Registry Numbers: 0
Heading Mapped to: *Night Blindness; *Eye Diseases, Hereditary
Frequency: 1
Note: mutation in GNAT1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Night Blindness, Congenital Stationary, Autosomal Dominant 3 MeSH Supplementary Concept Data 2025