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 Red eye
  1. SLC4A1 gene 
    ... of hereditary spherocytosis, resulting from the breakdown of red blood cells, include yellowing of the skin and whites of the eyes (jaundice), gallstones, and an enlarged spleen (splenomegaly). More ...
    https://medlineplus.gov/genetics/gene/slc4a1 - Genetics
  2. GNAQ gene 
    ... and often leads to three major features: a red or pink birthmark called a port-wine birthmark, brain abnormalities, and increased pressure in the eye (glaucoma) or other eye problems. The GNAQ gene ...
    https://medlineplus.gov/genetics/gene/gnaq - Genetics
  3. PKLR gene 
    ... and a molecule called bilirubin are released when red blood cells are destroyed, resulting in an excess of these substances circulating in the blood. Excess bilirubin in the blood causes yellowing of the eyes and skin (jaundice) and increases the risk of ...
    https://medlineplus.gov/genetics/gene/pklr - Genetics
  4. MC1R gene 
    ... oculocutaneous albinism type 2; however, they typically have red hair instead of the usual yellow, blond, or light brown hair seen with this condition. ... NCBI Gene ClinVar ...
    https://medlineplus.gov/genetics/gene/mc1r - Genetics
  5. GALE gene 
    ... such as clouding of the lens of the eye (cataract), intellectual disability, and damage to the liver, kidneys, and brain.Other mutations in the GALE gene reduce the activity of UDP-galactose-4-epimerase in red blood cells only. These genetic changes underlie a ...
    https://medlineplus.gov/genetics/gene/gale - Genetics
  6. FTL gene 
    ... Iron is needed for the body to produce red blood cells. ... the lenses of the eyes (cataracts) in infancy.The mutations that cause hyperferritinemia- ...
    https://medlineplus.gov/genetics/gene/ftl - Genetics
  7. OPN1LW gene 
    ... of genetic changes involving the OPN1LW gene cause red-green color vision defects, a form of color ... difficult or impossible to distinguish between shades of red, yellow, and green. Most red-green color vision ...
    https://medlineplus.gov/genetics/gene/opn1lw - Genetics
  8. OPN1MW gene 
    ... to light at long wavelengths (in the orange/red part of the visible spectrum). A nearby region ... of genetic changes involving the OPN1MW gene cause red-green color vision defects, a form of color ...
    https://medlineplus.gov/genetics/gene/opn1mw - Genetics
  9. HBA2 gene 
    ... protein called hemoglobin, which is the protein in red blood cells that carries oxygen to cells and ... molecule called heme. Heme molecules are necessary for red blood cells to pick up oxygen in the ...
    https://medlineplus.gov/genetics/gene/hba2 - Genetics
  10. HBA1 gene 
    ... protein called hemoglobin, which is the protein in red blood cells that carries oxygen to cells and ... molecule called heme. Heme molecules are necessary for red blood cells to pick up oxygen in the ...
    https://medlineplus.gov/genetics/gene/hba1 - Genetics
previous · 1 · 2 · next