Fetal Erythroblastosis

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.

Also Known As:

Erythroblastosis Fetalis; Newborn Hemolytic Disease; Erythroblastosis, Fetal; Erythroblastoses, Fetal; Erythroblastosis Fetali; Fetal Erythroblastoses; Fetali, Erythroblastosis; Fetalis, Erythroblastosis; Newborn Hemolytic Diseases; Hemolytic Disease of Newborn

Urogenital Diseases: 126
- Female Urogenital Diseases and Pregnancy Complications
  - Pregnancy Complications: 2961
    - Fetal Diseases: 814
      - Fetal Erythroblastosis: 297
Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Fetal Erythroblastosis: 297
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Fetal Diseases: 814
  - Fetal Erythroblastosis: 297
- Diseases Newborn Infant: 266
  - Fetal Erythroblastosis: 297
Immune System Diseases: 4321
- Fetal Erythroblastosis: 297

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Drug/Important Bio-Agent (IBA)

Therapy/Procedure