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Results 1 - 10 of 287 for Red
  1. Myoclonic epilepsy with ragged-red fibers 
    Myoclonic epilepsy with ragged-red fibers (MERRF) is a disorder that affects many parts of the body, particularly the muscles and nervous system. In most ... abnormal. These abnormal muscle cells are called ragged-red fibers. Other features of MERRF include recurrent seizures ( ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  2. 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
  3. Diamond-Blackfan anemia 
    ... bone marrow malfunctions and fails to make enough red blood cells, which carry oxygen to the body's tissues. The resulting shortage of red blood cells (anemia) usually becomes apparent during the ...
    https://medlineplus.gov/genetics/condition/diamond-blackfan-anemia - Genetics
  4. Sialidosis 
    ... Sialidosis type I, also referred to as cherry-red spot myoclonus syndrome, is the less severe form ... night blindness. An eye abnormality called a cherry-red spot, which can be identified with an eye ...
    https://medlineplus.gov/genetics/condition/sialidosis - Genetics
  5. PKLR gene 
    ... is active (expressed) in the liver and in red blood cells, where it provides instructions for producing ... enzyme function, causing a shortage of ATP in red blood cells and increased levels of other molecules ...
    https://medlineplus.gov/genetics/gene/pklr - Genetics
  6. Hereditary spherocytosis 
    Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells (anemia), yellowing of the eyes and skin (jaundice), and ...
    https://medlineplus.gov/genetics/condition/hereditary-spherocytosis - Genetics
  7. Glucose-6-phosphate dehydrogenase deficiency 
    ... dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs ... an enzyme called glucose-6-phosphate dehydrogenase causes red blood cells to break down prematurely. This destruction ...
    https://medlineplus.gov/...cose-6-phosphate-dehydrogenase-deficiency - Genetics
  8. Pyruvate kinase deficiency 
    ... kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the body' ... condition known as chronic hemolytic anemia, in which red blood cells are broken down (undergo hemolysis) prematurely, ...
    https://medlineplus.gov/.../condition/pyruvate-kinase-deficiency - Genetics
  9. Familial erythrocytosis 
    ... inherited condition characterized by an increased number of red blood cells (erythrocytes). The primary function of these ... dizziness, nosebleeds, and shortness of breath. The excess red blood cells also increase the risk of developing ...
    https://medlineplus.gov/genetics/condition/familial-erythrocytosis - Genetics
  10. Congenital dyserythropoietic anemia 
    ... inherited blood disorder that affects the development of red blood cells. This disorder is one of many ... is a condition characterized by a shortage of red blood cells. This shortage prevents the blood from ...
    https://medlineplus.gov/.../congenital-dyserythropoietic-anemia - Genetics
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