MeSH Browser

MeSH Supplementary: Night blindness, congenital stationary
Unique ID: C536122
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536122
Entry Term(s): CRSD; CSNB, Complete, X-Linked; CSNB, Incomplete, Autosomal Recessive; CSNB, Incomplete, X-Linked; CSNB1A; CSNB1B; CSNB2; CSNB2A; CSNB2B; Cone-rod synaptic disorder, congenital nonprogressive; Congenital stationary night blindness; Hemeralopia-myopia; Myopia-night blindness; Night Blindness, Congenital Stationary, Complete, Autosomal Recessive; Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive; Night Blindness, Congenital Stationary, Type 1A; Night Blindness, Congenital Stationary, Type 1B; Night Blindness, Congenital Stationary, Type 2; Night Blindness, Congenital Stationary, Type 2A; Night Blindness, Congenital Stationary, Type 2B; Night blindness, congenital stationary, type 1; Night blindness, congenital stationary, with myopia; X-Linked Csnb; X-linked congenital stationary night blindness; Xlcsnb
Registry Numbers: 0
Heading Mapped to: *Myopia; *Night Blindness; *Eye Diseases, Hereditary; *Genetic Diseases, X-Linked
Frequency: 150
Note: A clinically and genetically heterogeneous group of nonprogressive retinal disorders that are characterized by impaired NIGHT VISION, decreased VISUAL ACUITY; NYSTAGMUS; MYOPIA, and STRABISMUS. CSNB can be classified into 2 groups based on ELECTRORETINOGRAPHY findings. Germline mutations in several genes have been identified. OMIM: 310500
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Night blindness, congenital stationary Preferred

Night Blindness, Congenital Stationary, Type 1A Narrower

Night Blindness, Congenital Stationary, Type 2A Narrower

Night Blindness, Congenital Stationary, Type 1B Narrower

Night Blindness, Congenital Stationary, Type 2B Narrower

Night blindness, congenital stationary, type 1 Narrower

X-Linked Csnb Narrower

Cone-rod synaptic disorder, congenital nonprogressive Narrower

Night blindness, congenital stationary MeSH Supplementary Concept Data 2025