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Thalassemia

More information in Books or onNLM PubMed
Definition: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.  a congen hemolytic anemia; GEN or unspecified: prefer specifics; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES   
Examples alpha-Thalassemia; beta-Thalassemia; delta-Thalassemia
Other names Thalassemias
 
SubstanceCAS Registry & nameCategoriesSource
hemoglobin Medicine Lake  0   *Hemoglobins, Abnormal Thalassemia. J Clin Invest 1995 Feb;95(2):503-9

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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