Hereditary spherocytosis/Related Articles: Difference between revisions
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Latest revision as of 11:00, 27 August 2024
- See also changes related to Hereditary spherocytosis, or pages that link to Hereditary spherocytosis or to this page or whose text contains "Hereditary spherocytosis".
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Auto-populated based on Special:WhatLinksHere/Hereditary spherocytosis. Needs checking by a human.
- Anemia [r]: A condition characterized by insufficient circulating and effective hemoglobin in blood to support normal physiology. [e]
- Gene therapy [r]: Treatment of certain disorders, especially those caused by genetic anomalies or deficiencies, by introducing specific engineered genes into a patient's cells. [e]
- Iron [r]: An important transition metal and chemical element with the symbol Fe (Latin: ferrum) and atomic number 26. [e]
- Mutation [r]: Changes to the DNA sequence that cause new genetic variation. [e]
- Online Mendelian Inheritance in Man [r]: Curated database that catalogues all the known diseases with a genetic component, and links them to the relevant genes in the human genome. [e]
- Red blood cells [r]: Also called erythrocytes; a type of disc-shaped blood cell that contain hemoglobin, and the body's principal means of delivering oxygen to the body's cells via the blood, and the removal of carbon dioxide wastes that result from metabolism. [e]
- Neurotoxin [r]: A poison that acts on the nervous system. [e]
- Vitamin C [r]: Required by a few mammalian species, including humans and higher primates. It is water-soluble and is usually obtained by eating fruits and vegetables; associated with scurvy (hence its chemical name, ascorbic acid). [e]