Congenital plasminogen activator inhibitor deficiency type 1   717407006

SNOMED CT code


SNOMED code717407006
nameCongenital plasminogen activator inhibitor deficiency type 1
statusactive
date introduced2016-07-31
fully specified name(s)Congenital plasminogen activator inhibitor deficiency type 1 (disorder)
synonymsCongenital plasminogen activator inhibitor deficiency type 1
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
OccurrenceCongenital   255399007
parents
  • Hereditary coagulation factor deficiency   16922007
  • Congenital disease   66091009
  • Autosomal recessive hereditary disorder   85995004
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
            Congenital plasminogen activator inhibitor deficiency type 1   717407006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital plasminogen activator inhibitor deficiency type 1   717407006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Congenital plasminogen activator inhibitor deficiency type 1   717407006

ancestors
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