Pure red cell aplasia   50715003

SNOMED CT code


SNOMED code50715003
namePure red cell aplasia
statusactive
date introduced2002-01-31
fully specified name(s)Pure red cell aplasia (disorder)
synonyms
  • Red cell hypoplasia
  • Pure red cell anaemia
  • Pure red cell aplasia
  • Primary red cell aplasia
  • Pure red cell anemia
attributes - group2
Associated morphologyAplasia   45486003
Finding siteStructure of erythropoietic tissue   52901003
attributes - group1
InterpretsRed blood cell count   14089001
Has interpretationBelow reference range   281300000
parents
children
  • Acquired red cell aplasia   234376007
  • Acute pure red cell aplasia   57192008
  • Constitutional red cell aplasia and hypoplasia   267525005  removed: 2021-01-31
  • Pure red cell aplasia, acquired   234370001  removed: 2021-07-31
  • Secondary red cell aplasia NEC   234369002  removed: 2010-01-31
  • Transient erythroblastopenia of childhood   234375006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of hematopoietic structure   414027002
          Bone marrow disorder   127035006
            Pure red cell aplasia   50715003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Procedure related finding   127325009
      Evaluation finding   441742003
        Measurement finding   118245000
          Red blood cell count - finding   365625004
            Red blood cell count outside reference range   165427000
              Red blood cell count below reference range   165423001
                Pure red cell aplasia   50715003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Pure red cell aplasia   50715003

ancestors
sorted most to least specific
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