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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Hemoglobinopathies > Anemia, Sickle Cell > Hemoglobin SC Disease
Hemic and Lymphatic Diseases > Hematologic Diseases > Hemoglobinopathies > Anemia, Sickle Cell > Hemoglobin SC Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Anemia, Sickle Cell > Hemoglobin SC Disease
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Anemia, Sickle Cell > Hemoglobin SC Disease

Término preferido

Hemoglobin SC Disease  

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Tipo

  • mesh:Descriptor

Definición

  • One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.

Concepto genérico

Etiquetas alternativas

  • SC Disease
  • Sickle Cell Hemoglobin C Disease

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-XXD7495D-R

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RDF/XML TURTLE JSON-LD Creado 3/5/83, última modificación 25/7/01