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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Anemia, Hemolytic, Congenital > Spherocytosis, Hereditary
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Anemia > Anemia, Hemolytic > Anemia, Hemolytic, Congenital > Spherocytosis, Hereditary

Preferred term

Spherocytosis, Hereditary  

Type

  • Topical Descriptor

Broader concept

Related concepts

Scope note

  • A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.

In other languages

  • perinnöllinen pallosoluisuus

    Finnish

  • akoluurinen keltaisuus
  • akoluurinen suvuittainen keltaisuus
  • familiar ikterus med urin utan gallfärg
  • hereditaarinen sferosytoosi
  • hereditär sfärocytos
  • hereditäärinen sferosytoosi
  • icterus acholuricus
  • icterus familialis acholuricus
  • icterus haemolyticus sphaerocyticus congenitus
  • kongenital sfärocytisk hemolytisk ikterus
  • Minkowski-Chauffard
  • Minkowski-Chauffardin oireyhtymä
  • Minkowski-Chauffardin syndrooma
  • Minkowski-Chauffards syndrom
  • perinnöllinen sferosytoosi
  • periytyvä sferosytoosi
  • sphaerocytosis hereditaria
  • syndroma Minkowski-Chauffard
  • synnynnäinen pallosoluanemia
  • synnynnäinen pallosoluinen hemolyyttinen keltaisuus
  • synnynnäinen sferosytoosi
  • Hereditär sfärocytos

    Swedish

  • Ärftlig sfärocytos

URI

http://www.yso.fi/onto/mesh/D013103

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