SNOMED CT Concept  138875005

Clinical finding  404684003

Procedure related finding  127325009

Evaluation finding  441742003

Genetic finding  106221001

Phenotype  8116006

Blood group phenotype  115940004

ABO group phenotype  112143006

Blood group B  112149005

Blood group B variant  131158008

Blood group B>el<   131161009

SNOMED CT code


SNOMED code131161009
nameBlood group B>el<
statusactive
date introduced2002-01-31
fully specified name(s)Blood group B>el< (finding)
synonymsBlood group B>el<
attributes - group2
InterpretsGenetic test   405824009
attributes - group1
InterpretsBlood transfusion test   252314007
parentsBlood group B variant   131158008
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
              ABO group phenotype   112143006
                Blood group B   112149005
                  Blood group B variant   131158008
                    Blood group B>el<   131161009

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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