SNOMED CT Concept  138875005

Clinical finding  404684003

Functional finding  118228005

Disorder of hemostatic system  362970003

Blood coagulation disorder  64779008

Fibrinogen abnormality  234455001

Hyperfibrinogenemia  439000005

Hereditary hyperfibrinogenemia   440924009

SNOMED CT code


SNOMED code440924009
nameHereditary hyperfibrinogenemia
statusactive
date introduced2009-01-31
fully specified name(s)Hereditary hyperfibrinogenemia (disorder)
synonyms
  • Congenital hyperfibrinogenemia
  • Hereditary hyperfibrinogenaemia
  • Hereditary hyperfibrinogenemia
  • Congenital hyperfibrinogenaemia
attributes - group2
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
attributes - group1
InterpretsFibrinogen assay, quantitative   6668007
Has interpretationAbove reference range   281302008
parents
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
          Fibrinogen abnormality   234455001
            Hyperfibrinogenemia   439000005
              Hereditary hyperfibrinogenemia   440924009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Thrombophilia   234467004
          Hereditary thrombophilia   439698008
            Hereditary hyperfibrinogenemia   440924009

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