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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Hemoglobinopathies > Thalassemia > alpha-Thalassemia
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemoglobinopathies > Thalassemia > alpha-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Thalassemia > alpha-Thalassemia
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Thalassemia > alpha-Thalassemia

Término preferido

alpha-Thalassemia  

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Tipo

  • mesh:Descriptor

Definición

  • A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.

Concepto genérico

Conceptos específicos

Conceptos relacionados

Etiquetas alternativas

  • Alpha Thalassemia
  • A-Thalassemia
  • Hemoglobin H Disease
  • Thalassemia-alpha

En otras lenguas

  • alpha-Thalassémie

    francés

  • a-Thalassémie
  • Hémoglobinopathie H
  • Hémoglobinose H
  • Thalassémie alpha

URI

http://data.loterre.fr/ark:/67375/JVR-LR1F1G0M-0

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RDF/XML TURTLE JSON-LD Creado 7/5/92, última modificación 8/7/13