Hemolytic disease of fetus or newborn due to isoimmunization (disorder)
SCTID: 111468003, Primitive, Inactive
111468003|Hemolytic disease of fetus or newborn due to isoimmunization (disorder)|
- en Alloimmune haemolytic disease of newborn
- en Alloimmune hemolytic disease of newborn
- en Erythroblastosis fetalis
- en Erythroblastosis neonatorum
- en Haemolytic disease of foetus and newborn due to isoimmunisation
- en Haemolytic disease of the newborn
- en Hemolytic disease of fetus and newborn due to isoimmunization
- en Hemolytic disease of the newborn
- en Isoimmunisation of newborn
- en Isoimmunization of newborn
- en Neonatal anaemia
- en Neonatal anemia
- en Perinatal anaemia
- en Perinatal anemia
- en Haemolytic disease of foetus or newborn
- en Haemolytic disease of foetus or newborn due to isoimmunisation
- en Hdn - hemolytic disease of the newborn
- en Ef - erythroblastosis fetalis
- en Hdn - haemolytic disease of the newborn
- en Hemolytic disease of fetus or newborn
- en Hemolytic disease of fetus or newborn due to isoimmunization
- en Hemolytic disease of fetus or newborn due to isoimmunization (disorder)