SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Hereditary coagulation factor deficiency  16922007

Hereditary factor XIII deficiency disease  50189006

Hereditary factor XIII A subunit deficiency   439455002

SNOMED CT code


SNOMED code439455002
nameHereditary factor XIII A subunit deficiency
statusactive
date introduced2009-01-31
fully specified name(s)Hereditary factor XIII A subunit deficiency (disorder)
synonyms
  • Hereditary factor XIII A subunit deficiency
  • Hereditary factor XIII type II deficiency
  • Hereditary factor XIII alpha subunit deficiency
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parentsHereditary factor XIII deficiency disease   50189006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary coagulation factor deficiency   16922007
            Hereditary factor XIII deficiency disease   50189006
              Hereditary factor XIII A subunit deficiency   439455002

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

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.