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 Number: 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 1 Narrower

X-Linked Csnb Narrower

Night Blindness, Congenital Stationary, Type 1B Narrower

Night Blindness, Congenital Stationary, Type 2A Narrower

Night Blindness, Congenital Stationary, Type 2B Narrower

Cone-rod synaptic disorder, congenital nonprogressive Narrower

Night Blindness, Congenital Stationary, Type 1A Narrower

Night blindness, congenital stationary MeSH Supplementary Concept Data 2024