| Descriptor English: | Erythroblastosis, Fetal | ||||||
| Descriptor Spanish: |
Eritroblastosis Fetal
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| Descriptor Portuguese: | Eritroblastose Fetal | ||||||
| Descriptor French: | Érythroblastose du nouveau-né | ||||||
| Entry term(s): |
Erythroblastoses, Fetal Erythroblastosis Fetali Erythroblastosis Fetalis Fetal Erythroblastoses Fetal Erythroblastosis Fetali, Erythroblastosis Fetalis, Erythroblastosis Hemolytic Disease of Newborn Newborn Hemolytic Disease Newborn Hemolytic Diseases |
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| Tree number(s): |
C12.050.703.277.060 C15.378.295 C16.300.060 C16.614.304 C20.306 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D004899 | ||||||
| Scope note: | 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. |
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| Annotation: | erythroblastosis, non-fetal may be ERYTHREMIC MYELOSIS but be careful; do not confuse with VITAMIN K DEFICIENCY BLEEDING |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Related: |
Jaundice, Neonatal
MeSH | ||||||
| DeCS ID: | 4985 | ||||||
| Unique ID: | D004899 | ||||||
| NLM Classification: | WH 425 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1966/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2009/07/06 |
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Erythroblastosis, Fetal
- Preferred
| Concept UI |
M0007688 |
| Scope note | 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. |
| Preferred term | Erythroblastosis, Fetal |
| Entry term(s) |
Erythroblastoses, Fetal Erythroblastosis Fetali Erythroblastosis Fetalis Fetal Erythroblastoses Fetal Erythroblastosis Fetali, Erythroblastosis Fetalis, Erythroblastosis Hemolytic Disease of Newborn Newborn Hemolytic Disease Newborn Hemolytic Diseases |
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