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Blind
- Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- Autosomal dominant congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
- X-linked congenital stationary night blindness is a disorder of the retina, which is a specialized tissue at the back of the eye that detects light and ...
- ... forms of color vision deficiency (also called color blindness), in which people can perceive color but have ... of the condition. Achromatism Rod monochromatism Total color blindness Genetic Testing Registry: Achromatopsia Genetic Testing Registry: Achromatopsia ...
- Color vision deficiency (sometimes called color blindness) represents a group of conditions that affect the perception of color. Red-green color vision defects are the most common form of ...
- ... is an inherited eye disorder that leads to blindness in male infants at birth or soon after ... hereditaria Congenital progressive oculo-acoustico-cerebral degeneration Episkopi blindness Fetal iritis syndrome Norrie syndrome Norrie's disease ...
- 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, ...
- 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 ...
- ... visual acuity) slowly worsens, often leading to legal blindness in mid-adulthood.People with this condition may ... traits to their sons. Deafness syndrome, progressive, with blindness, dystonia, fractures, and mental deficiency Deafness-dystonia-optic ...
- ... impaired ability to see in low light (night blindness) and the presence of whitish-yellow flecks in ... eye examination.Individuals with fundus albipunctatus experience night blindness from an early age. In particular, they have ...