SNOMED CT Concept  138875005

Clinical finding  404684003

Functional finding  118228005

Disorder of hemostatic system  362970003

Platelet disorder  22716005

Inherited platelet disorder   234469001

SNOMED CT code


SNOMED code234469001
nameInherited platelet disorder
statusactive
date introduced2002-01-31
fully specified name(s)Inherited platelet disorder (disorder)
synonyms
  • Hereditary thrombocytopathy
  • Hereditary platelet disorder
  • Inherited platelet disorder
attributes - group2
Has interpretationAbnormal   263654008
InterpretsHemostatic function   74848003
attributes - group1
Finding siteBody system structure   91689009
parents
  • Platelet disorder   22716005
  • Hereditary disorder of cellular element of blood   414393003
children
  • Ataxia pancytopenia syndrome   768556005
  • Familial thrombocytosis   720950009
  • Giant platelet syndrome   234478007
  • Hereditary isolated aplastic anemia   783255002
  • Hereditary platelet function disorder   128096008
  • Hereditary thrombocytopenic disorder   438492008
  • Pancytopenia with developmental delay syndrome   774071007
  • Platelet membrane defect   234470000
  • Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome   721882001
  • Revesz syndrome   723512008
  • Thrombocythemia with distal limb defect   771511005
  • Thromboxane generation defect   234475005
  • Upshaw-Schulman syndrome   373420004
  • WT limb blood syndrome   719019000
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Hereditary disorder of cellular element of blood   414393003
          Inherited platelet disorder   234469001

ancestors
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cpt crosswalks

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