Night blindness, congenital stationary [Supplementary Concept]
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 introduced: August 25, 2010
MeSH Unique ID: C536122
Heading Mapped to:
Entry Terms:
- Congenital stationary night blindness
- Night Blindness, Congenital Stationary, Type 1A
- Night blindness, congenital stationary, with myopia
- Hemeralopia-myopia
- Myopia-night blindness
- CSNB, Complete, X-Linked
- CSNB1A
- Night Blindness, Congenital Stationary, Type 2A
- X-linked congenital stationary night blindness
- Night Blindness, Congenital Stationary, Type 2
- CSNB2A
- CSNB2
- CSNB, Incomplete, X-Linked
- Night Blindness, Congenital Stationary, Type 1B
- Night Blindness, Congenital Stationary, Complete, Autosomal Recessive
- CSNB1B
- Night Blindness, Congenital Stationary, Type 2B
- Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive
- CSNB2B
- CSNB, Incomplete, Autosomal Recessive
- Night blindness, congenital stationary, type 1
- X-Linked Csnb
- Xlcsnb
- Cone-rod synaptic disorder, congenital nonprogressive
- CRSD