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

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delta-Thalassemia  

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Tipo

  • mesh:Descriptor

Definición

  • A hereditary disorder characterized by reduced or absent DELTA-GLOBIN thus effecting the level of HEMOGLOBIN A2, a minor component of adult hemoglobin monitored in the diagnosis of BETA-THALASSEMIA.

Concepto genérico

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URI

http://data.loterre.fr/ark:/67375/JVR-BJDG95VP-M

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RDF/XML TURTLE JSON-LD Creado 8/7/08