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Concept information

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

Terme préférentiel

Anemia, Dyserythropoietic, Congenital  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Synonyme(s)

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

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-F25P9R69-R

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RDF/XML TURTLE JSON-LD Date de création 23/04/1979, dernière modification le 08/07/2013