"Erythroblastosis, Fetal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D004899
|
| MeSH Number(s) |
C13.703.277.060 C15.378.295 C16.300.060 C16.614.304 C20.306
|
| Concept/Terms |
Erythroblastosis, Fetal- Erythroblastosis, Fetal
- Erythroblastoses, Fetal
- Fetal Erythroblastoses
- Fetal Erythroblastosis
- Erythroblastosis Fetalis
- Erythroblastosis Fetali
- Fetali, Erythroblastosis
- Fetalis, Erythroblastosis
- Hemolytic Disease of Newborn
- Newborn Hemolytic Disease
- Newborn Hemolytic Diseases
|
Below are MeSH descriptors whose meaning is more general than "Erythroblastosis, Fetal".
Below are MeSH descriptors whose meaning is more specific than "Erythroblastosis, Fetal".
This graph shows the total number of publications written about "Erythroblastosis, Fetal" by people in this website by year, and whether "Erythroblastosis, Fetal" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 1 | 0 | 1 |
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Below are the most recent publications written about "Erythroblastosis, Fetal" by people in Profiles.
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Perry GH, Xue Y, Smith RS, Meyer WK, Caliskan M, Yanez-Cuna O, Lee AS, Guti?rrez-Arcelus M, Ober C, Hollox EJ, Tyler-Smith C, Lee C. Evolutionary genetics of the human Rh blood group system. Hum Genet. 2012 Jul; 131(7):1205-16.