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Terminology chevron_right Concepts chevron_right 206430005

Production
The component that hold information about this concept.
(haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn) (disorder)
Erythroblastosis fetalis
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

(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)

206430005 |(haemolytic disease due to rhesus isoimmunisation) or (erythroblastosis fetalis) or (rhesus isoimmunisation of the newborn) (disorder)|

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