SNOMED CT Concept  138875005

Clinical finding  404684003

Procedure related finding  127325009

Evaluation finding  441742003

Genetic finding  106221001

Phenotype  8116006

Blood group phenotype  115940004

P blood group phenotype  115794002

p phenotype  24403008

P>2< phenotype   103225004

SNOMED CT code


SNOMED code103225004
nameP>2< phenotype
statusactive
date introduced2002-01-31
fully specified name(s)P>2< phenotype (finding)
synonyms
  • Blood group P>2<
  • P>2< phenotype
attributes - group2
InterpretsGenetic test   405824009
attributes - group1
InterpretsBlood transfusion test   252314007
parentsp phenotype   24403008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Procedure related finding   127325009
      Evaluation finding   441742003
        Genetic finding   106221001
          Phenotype   8116006
            Blood group phenotype   115940004
              P blood group phenotype   115794002
                p phenotype   24403008
                  P>2< phenotype   103225004

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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