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

Término preferido

beta-Thalassemia  

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Tipo

  • mesh:Descriptor

Definición

  • A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.

Concepto genérico

Etiquetas alternativas

  • beta Thalassemia
  • Microcytemia, beta Type
  • Thalassemia, beta Type

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-FD2D24W6-2

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