Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency   783250007

SNOMED CT code


SNOMED code783250007
nameHereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
statusactive
date introduced2019-07-31
fully specified name(s)Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (disorder)
synonymsHereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
OccurrenceCongenital   255399007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency   783250007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Thrombophilia   234467004
          Hereditary thrombophilia   439698008
            Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency   783250007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency   783250007

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