SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital fibrinogen abnormality  234456000

Dysfibrinogenemia   111589005

SNOMED CT code


SNOMED code111589005
nameDysfibrinogenemia
statusactive
date introduced2002-01-31
fully specified name(s)Dysfibrinogenemia (disorder)
synonyms
  • Dysfibrinogenemia
  • Dysfibrinogenaemia
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
attributes - group2
OccurrenceCongenital   255399007
parents
children
  • Alpha chain defect dysfibrinogenemia   234459007
  • Beta chain defect dysfibrinogenemia   234460002
  • Congenital dysfibrinogenemia   45366001
  • Gamma chain defect dysfibrinogenemia   234461003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital fibrinogen abnormality   234456000
          Dysfibrinogenemia   111589005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Blood coagulation disorder   64779008
          Coagulation factor deficiency syndrome   86075001
            Factor I deficiency disease   439458000
              Dysfibrinogenemia   111589005

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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