SNOMED CT Concept  138875005

Clinical finding  404684003

Functional finding  118228005

Disorder of hemostatic system  362970003

Thrombophilia  234467004

Hereditary thrombophilia  439698008

Factor V Leiden mutation   307091009

SNOMED CT code


SNOMED code307091009
nameFactor V Leiden mutation
statusactive
date introduced2002-01-31
fully specified name(s)Factor V Leiden mutation (disorder)
synonyms
  • Factor 5 Leiden mutation
  • Factor V Leiden mutation
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parentsHereditary thrombophilia   439698008
children
  • Heterozygous Factor V Leiden mutation   307116001
  • Homozygous Factor V Leiden mutation   307115002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Thrombophilia   234467004
          Hereditary thrombophilia   439698008
            Factor V Leiden mutation   307091009

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.

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