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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Erythroblastosis, Fetal
Immune System Diseases > Erythroblastosis, Fetal
Hemic and Lymphatic Diseases > Hematologic Diseases > Erythroblastosis, Fetal
Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Pregnancy Complications > Fetal Diseases > Erythroblastosis, Fetal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Fetal Diseases > Erythroblastosis, Fetal

Terme préférentiel

Erythroblastosis, Fetal  

Type

  • mesh:Descriptor

Définition

  • A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN.

Concept générique

Concepts spécifiques

Concepts associés

Synonyme(s)

  • Erythroblastosis Fetalis
  • Hemolytic Disease of Newborn

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-F5QMLCFQ-L

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RDF/XML TURTLE JSON-LD Date de création 01/01/1999, dernière modification le 30/06/2021