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

Preferred term

Anemia, Dyserythropoietic, Congenital  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Anemia, Congenital Dyserythropoietic
  • Anemias, Congenital Dyserythropoietic
  • Congenital Dyserythropoietic Anemia
  • Congenital Dyserythropoietic Anemias
  • Dyserythropoietic Anemia, Congenital
  • Dyserythropoietic Anemias, Congenital

Scope note

  • A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.

History note

  • 1991(1980); use ANEMIA, HEMOLYTIC, CONGENITAL 1980-1990

In other languages

  • synnynnäinen dyserytropoieettinen anemia

    Finnish

  • anaemia dyserythropoetica congenita
  • anaemia dyserythropoietica congenita
  • anaemia dyshaematopoetica
  • anaemia dyshematopoietica congenita
  • dyshematopoieettinen anemia
  • kongenitaalinen dyserytropoieettinen anemia
  • kongenital dyserytropoetisk anemi
  • kongenital dyshematopoetisk anemi
  • synnynnäinen dyshematopoieettinen anemia
  • Medfödd dyserytropoietisk anemi

    Swedish

  • Anemi, dyserytropoietisk, medfödd
  • Kongenital dyserytropoetisk anemi

URI

http://www.yso.fi/onto/mesh/D000742

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