congenital stationary Night blindness

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

Also Known As:

Night blindness, congenital stationary; 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

Eye Diseases: 3522
- Refractive Errors: 3499
  - Myopia: 8363
    - congenital stationary Night blindness: 198
- Vision Disorders: 2977
  - Night Blindness: 432
    - congenital stationary Night blindness: 198
- Hereditary Eye Diseases: 18
  - congenital stationary Night blindness: 198
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - X-Linked Genetic Diseases: 42
    - congenital stationary Night blindness: 198
  - Hereditary Eye Diseases: 18
    - congenital stationary Night blindness: 198

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Disease

Drug/Important Bio-Agent (IBA)