(haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn) (disorder)
SCTID: 206430005, Primitive, Inactive
206430005|(haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn) (disorder)|
- en (haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn) (disorder)
- en Erythroblastosis fetalis
- en Haemolytic disease due to rhesus isoimmunisation
- en Hemolytic disease due to rhesus isoimmunization
- en (haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn)
- en Rhesus isoimmunisation of the newborn
- en Rhesus isoimmunization of the newborn
- en (hemolytic disease due to rhesus isoimmunization) or (erythroblastosis fetalis) or (rhesus isoimmunization of the newborn)