SNOMED CT Concept  138875005

Clinical finding  404684003

Functional finding  118228005

Disorder of hemostatic system  362970003

Blood coagulation disorder  64779008

von Willebrand disorder  128105004

Hereditary von Willebrand disease  1259242002

Hereditary von Willebrand disease type 2   128107007

SNOMED CT code


SNOMED code128107007
nameHereditary von Willebrand disease type 2
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary von Willebrand disease type 2 (disorder)
synonyms
  • von Willebrand disease type 2
  • Hereditary von Willebrand disease type 2
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parentsHereditary von Willebrand disease   1259242002
children
  • Hereditary von Willebrand disease type 2A   359711001
  • Hereditary von Willebrand disease type 2B   359717002
  • Hereditary von Willebrand disease type 2M   359725000
  • Hereditary von Willebrand disease type 2N   359732009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Blood coagulation disorder   64779008
          von Willebrand disorder   128105004
            Hereditary von Willebrand disease   1259242002
              Hereditary von Willebrand disease type 2   128107007

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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