Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

SNOMED CT code


SNOMED code1172901009
nameCytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
statusactive
date introduced2021-09-30
fully specified name(s)Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder)
synonyms
  • PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction
  • PLA2G4A-related platelet dysfunction
  • Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency
  • Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
attributes - group3
Clinical courseRecurrent   255227004
attributes - group2
Finding siteGastrointestinal tract structure   122865005
Associated morphologyUlcer   56208002
parents
  • Hereditary platelet function disorder   128096008
  • Digestive system hereditary disorder   363080007
  • Gastrointestinal ulcer   40845000
  • Recurrent disease   58184002
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Disorder of hemostatic system   362970003
        Platelet disorder   22716005
          Inherited platelet disorder   234469001
            Hereditary platelet function disorder   128096008
              Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Ulcer   429040005
        Gastrointestinal ulcer   40845000
          Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Recurrent disease   58184002
        Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder   1172901009

ancestors
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