Hereditary coagulation factor deficiency   16922007

SNOMED CT code


SNOMED code16922007
nameHereditary coagulation factor deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary coagulation factor deficiency (disorder)
synonymsHereditary coagulation factor deficiency
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parents
  • Hereditary disease   32895009
  • Coagulation factor deficiency syndrome   86075001
children
  • Congenital plasminogen activator inhibitor deficiency type 1   717407006
  • Familial multiple factor deficiency syndrome   81783000
  • Hereditary combined coagulation factor deficiency   439157002
  • Hereditary factor I deficiency disease   31925001
  • Hereditary factor II deficiency disease   33297000
  • Hereditary factor V deficiency disease   88776002
  • Hereditary factor VII deficiency syndrome   40855001
  • Hereditary factor VIII deficiency disease   28293008
  • Hereditary factor X deficiency disease   37350004
  • Hereditary factor XII deficiency disease   43217004
  • Hereditary factor XIII deficiency disease   50189006
  • Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome   733028000
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Blood coagulation disorder   64779008
          Coagulation factor deficiency syndrome   86075001
            Hereditary coagulation factor deficiency   16922007

ancestors
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