Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 20 for Blind
  1. MYO7A gene 
    The MYO7A gene provides instructions for making a protein called myosin VIIA, which is part of a group of proteins called unconventional myosins. These proteins, ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  2. CDH23 gene 
    The CDH23 gene provides instructions for making cadherin 23, a type of protein that helps cells stick together. Different versions of this protein are made ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  3. NYX gene 
    ... in people with X-linked congenital stationary night blindness. NYX gene variants are responsible for the complete ... characterized by difficulty seeing in low light (night blindness), loss of sharpness (reduced visual acuity), severe nearsightedness ( ...
    https://medlineplus.gov/genetics/gene/nyx - Genetics
  4. CACNA1F gene 
    ... in people with X-linked congenital stationary night blindness. CACNA1F gene variants are responsible for the incomplete ... also have difficulty seeing in low light (night blindness).Variants in the CACNA1F gene change the structure ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  5. RHO gene 
    ... found to cause autosomal dominant congenital stationary night blindness, which is characterized by a loss of vision ... pigmentosa (described below), autosomal dominant congenital stationary night blindness does not affect daytime vision.The RHO gene ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  6. GRM6 gene 
    ... found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
    https://medlineplus.gov/genetics/gene/grm6 - Genetics
  7. GNAT1 gene 
    ... found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... the brain as not meaningful, resulting in night blindness. More About This Health Condition CSNBAD3 GBT1 GNAT1_ ...
    https://medlineplus.gov/genetics/gene/gnat1 - Genetics
  8. PDE6B gene 
    ... found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... the brain as not meaningful, resulting in night blindness. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics
  9. TRPM1 gene 
    ... found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  10. RGS9 gene 
    ... cannot respond to light. This delay causes temporary blindness in response to changing light conditions and may ...
    https://medlineplus.gov/genetics/gene/rgs9 - Genetics
previous · 1 · 2 · next