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

Preferred term

Sickle Cell Trait  

Type

  • Topical Descriptor

Broader concept

Scope note

  • The condition of being heterozygous for hemoglobin S.

History note

  • 91(75); was see under ANEMIA, SICKLE CELL 1975-90

In other languages

  • sirppisoluanemian kantajuus

    Finnish

  • haemoglobinum heterozygoticum
  • Hb-S-kantajuus
  • hemoglobiini S -heterotsygoottisuus
  • heterotsygoottinen S-hemoglobiini
  • proprietas Hb-S
  • proprietas meniscocytica
  • sickle cell -kantajuus
  • Sicklecelltrait

    Swedish

URI

http://www.yso.fi/onto/mesh/D012805

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