Specific code 2012 ICD-9-CM Diagnosis Code 287.1
Qualitative platelet defects
  • Short description: Thrombocytopathy.
  • ICD-9-CM 287.1 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 287.1 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2012 version of ICD-9-CM 287.1.
  • More recent version(s) of ICD-9-CM 287.1: 2013 2014.
Disease Synonyms
  • Acquired PF-3 disease
  • Acquired platelet disorder
  • 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
  • Drug induced platelet dysfunction
  • 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 disorder, qualitative
  • Platelet dysfunction associated with uremia
  • Platelet dysfunction due to aspirin
  • Platelet dysfunction due to drugs
  • Platelet dysfunction, drug induced
  • 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
287.1 Excludes
  • von Willebrand's disease (286.4)
Applies To
  • Thrombasthenia (hemorrhagic) (hereditary)
  • Thrombocytasthenia
  • Thrombocytopathy (dystrophic)
  • Thrombopathy (Bernard-Soulier)
Convert to ICD-10-CM: 287.1 converts directly to:
  • 2014 ICD-10-CM D69.1 Qualitative platelet defects
ICD-9-CM Volume 2 Index entries containing back-references to 287.1:
  • Bernard-Soulier disease or thrombopathy 287.1
  • Defect, defective 759.9
    • platelet (qualitative) 287.1
  • Deficiency, deficient
    • platelet NEC 287.1
  • 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
    • Willebrand-J├╝rgens (angiohemophilia) 286.4
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 287.1 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.