SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Hereditary von Willebrand disease type 1  128106003

Hereditary von Willebrand disease type IA   359700009

SNOMED CT code


SNOMED code359700009
nameHereditary von Willebrand disease type IA
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary von Willebrand disease type 1A (disorder)
synonyms
  • Hereditary von Willebrand disease type 1A
  • Hereditary von Willebrand disease type IA
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parentsHereditary von Willebrand disease type 1   128106003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Hereditary von Willebrand disease type 1   128106003
                Hereditary von Willebrand disease type IA   359700009

ancestors
sorted most to least specific
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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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