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Terminology chevron_right Concepts chevron_right 111468003

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The component that hold information about this concept.
Hemolytic disease of fetus or newborn due to isoimmunization (disorder)
Neonatal anemia
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

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)

111468003 |Hemolytic disease of fetus or newborn due to isoimmunization (disorder)|

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