Hemolytic disease of fetus or newborn due to abo immunization (disorder)
SCTID: 32858009, Primitive, Active
32858009|Hemolytic disease of fetus or newborn due to abo immunization (disorder)|
- vi Bệnh tan máu ở thai nhi hoặc trẻ sơ sinh do sự tạo miễn dịch abo
- en Erythroblastosis fetalis due to abo isoimmunisation
- en Haemolytic disease of fetus or newborn due to abo immunisation
- en Erythroblastosis foetalis due to abo isoimmunisation
- en Haemolytic disease of foetus or newborn due to abo immunisation
- en Abo haemolytic disease of the newborn
- en Abo hdn - abo haemolytic disease of the newborn
- en Abo hdn - abo hemolytic disease of the newborn
- en Abo hemolytic disease of the newborn
- en Abo isoimmunisation of the newborn
- en Abo isoimmunization of the newborn
- en Anaemia due to abo incompatibility in the newborn
- en Anemia due to abo incompatibility in the newborn
- en Erythroblastosis fetalis due to abo isoimmunization
- en Haemolytic disease due to abo isoimmunisation
- en Hemolytic disease due to abo isoimmunization
- en Hemolytic disease of fetus or newborn due to abo immunization
- en Hemolytic disease of fetus or newborn due to abo immunization (disorder)
- en Jaundice due to abo isoimmunisation of the newborn
- en Jaundice due to abo isoimmunization of the newborn