01
CREB3L4
No data
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Erythroblastosis, Fetal
- Standard Disease Name
- erythroblastosis, fetal
- MeSH Tree
- No data
- ICD-10
- P55|P55.9
Identifiers
- DO ID
- No data
- MeSH ID
- D004899
- OMIM ID
- No data
- UMLS ID
- C0014761
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:A condition of the newborn characterized by the destruction of red blood cells initiated by the transmission of IgG antibodies from mother to child via the placenta.|NCI2016_02D:A disorder of the fetus or newborn that occurs when fetal cells that are coated with IgG alloantibodies from the mother attack antigens inherited from the father. Severity can range from absence of symptoms to death.|MSH2017_2016_08_12: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.|CSP2006:hemolytic anemia of the fetus or newborn caused by transplacental transmission of maternally formed antibody, usually secondary to an incompatibility between the blood groups of mother and offspring.
Related
Related Entities
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