287.1 THROMBOCYTOPATHY


Code Information

Diagnosis Code: 287.1

Short Description: Thrombocytopathy

Long Description: Qualitative platelet defects

Code Classification:

  • Diseases of the blood and blood-forming organs (280–289)
    • Diseases of the blood and blood-forming organs (280-289)
      • 287 Purpura and other hemorrhagic conditions
        • 287.1 Thrombocytopathy

Code Version: 2015 ICD-9-CM


Synonyms

  • Acquired platelet disorder
  • Acquired platelet factor 3 disease
  • Acquired platelet function disorder
  • Acquired storage pool deficiency
  • Bernard Soulier syndrome
  • Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type
  • Cyclooxygenase deficiency
  • Decreased platelet life span
  • Dense body defect
  • Exhausted platelets
  • Giant platelet syndrome
  • Glanzmann's thrombasthenia
  • Glycoprotein Ia defect
  • Glycoprotein Ib defect
  • Gray platelet syndrome
  • Hereditary platelet function disorder
  • Inherited platelet disorder
  • Isolated collagen aggregation defect
  • Megakaryocytic aplasia
  • Mixed alpha granule and dense body deficiency
  • Platelet dense granule deficiency
  • Platelet disorder
  • Platelet dysfunction associated with uremia
  • Platelet dysfunction due to aspirin
  • Platelet membrane defect
  • Platelet procoagulant activity deficiency
  • Platelet sequestration
  • Platelet storage pool defect
  • Platelet type pseudo-von Willebrand disease
  • Qualitative platelet disorder
  • Scott syndrome
  • Storage pool disease of platelets
  • Thromboxane generation defect
  • Thromboxane synthetase deficiency

References to Index of Diseases and Injuries

The code 287.1 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Bernard-Soulier disease or thrombopathy 287.1
  • Defect, defective 759.9
    • platelet (qualitative) 287.1
      • constitutional 286.4
  • Deficiency, deficient
    • platelet NEC 287.1
      • constitutional 286.4
  • Diacyclothrombopathia 287.1
  • Disease, diseased - see also Syndrome
    • Bernard-Soulier (thrombopathy) 287.1
    • Glanzmann's (hereditary hemorrhagic thrombasthenia) 287.1
    • Naegeli's 287.1
  • Disorder - see also Disease
    • platelets (blood) 287.1
  • Dysfunction
    • platelets (blood) 287.1
  • Glanzmann (-Naegeli) disease or thrombasthenia 287.1
  • Naegeli's
    • disease (hereditary hemorrhagic thrombasthenia 287.1
  • Thrombasthenia (Glanzmann's) (hemorrhagic) (hereditary) 287.1
  • Thromboasthenia (Glanzmann's) (hemorrhagic) (hereditary) 287.1
  • Thrombocytasthenia (Glanzmann's) 287.1
  • Thrombocytopathy (dystrophic) (granulopenic) 287.1
  • Thrombopathy (Bernard-Soulier) 287.1
    • constitutional 286.4
    • Willebrand-J�rgens (angiohemophilia) 286.4

Crosswalk Information

The code 287.1 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
287.1 Right Arrow D69.1 Qualitative platelet defects
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
287.0 Allergic purpura
287.2 Other nonthrombocytopenic purpuras
287.30 Primary thrombocytopenia,unspecified
287.31 Immune thrombocytopenic purpura
287.32 Evans' syndrome
287.33 Congenital and hereditary thrombocytopenic purpura
287.39 Other primary thrombocytopenia
287.41 Posttransfusion purpura
287.49 Other secondary thrombocytopenia
287.5 Thrombocytopenia, unspecified
287.8 Other specified hemorrhagic conditions
287.9 Unspecified hemorrhagic conditions


This page was last updated on: 10/1/2014