Diagnosis Code: D69.1

Short Description: Qualitative platelet defects

Long Description: Qualitative platelet defects

The code D69.1 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
    • Purpura and other hemorrhagic conditions (D69)
      • D69.1 Qualitative platelet defects

Code Version: 2022 ICD-10-CM

Synonyms

• Abnormal platelet destruction
• Abnormal platelet production
• Acquired PF-3 disease
• Acquired platelet disorder
• Acquired platelet function disorder
• Acquired platelet function disorder
• Acquired platelet function disorder
• Acquired platelet function disorder
• Acquired storage pool deficiency
• Asplenia
• Autoimmune state
• Autoplatelet sensitivity
• Autosensitivity
• Bernard Soulier syndrome
• Bleeding diathesis due to collagen receptor defect
• Congenital dyserythropoietic anemia
• Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type
• Congenital miosis
• Constricted pupil
• Cyclooxygenase deficiency
• Decreased platelet destruction
• Decreased platelet life span
• Dense body defect
• Dense body defect
• Exhausted platelets
• Familial alpha>2< adrenergic receptor defect in platelets
• Familial platelet syndrome with predisposition to acute myelogenous leukemia
• Giant platelet syndrome
• Giant platelet syndrome
• Glanzmann's thrombasthenia
• Glycoprotein Ia defect
• Glycoprotein Ib defect
• Glycoprotein VI deficiency
• Gray platelet syndrome
• Hereditary platelet function disorder
• Increased platelet destruction
• Ineffective thrombopoiesis
• Inherited platelet disorder
• Isolated collagen aggregation defect
• Medich giant platelet syndrome
• Mediterranean macrothrombocytopenia
• Megakaryocyte finding
• Megakaryocytic thrombocytopenia
• Mixed alpha granule and dense body deficiency
• Montreal platelet syndrome
• Platelet clumps
• Platelet dense granule deficiency
• Platelet disorder
• Platelet dysfunction associated with uremia
• Platelet dysfunction due to aspirin
• Platelet dysfunction due to drugs
• Platelet dysfunction due to drugs
• Platelet membrane defect
• Platelet morphology - finding
• Platelet morphology - finding
• Platelet procoagulant activity deficiency
• Platelet production finding
• Platelet satellite
• Platelet secretory disorder
• Platelet sequestration
• Platelet storage pool defect
• Qualitative platelet disorder
• Scott syndrome
• Sensitized cell
• Sensitized platelet
• Thrombocytopathy, asplenia and miosis
• Thromboxane generation defect
• Thromboxane synthetase deficiency
• White platelet syndrome
• X-linked dyserythropoietic anemia with abnormal platelets and neutropenia

References to Index of Diseases and Injuries

The code D69.1 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Bernard-Soulier [giant platelet] syndrome
  • Glanzmann's disease
  • Grey platelet syndrome
  • Thromboasthenia (hemorrhagic) (hereditary)
  • Thrombocytopathy
• Type 1 Excludes Notes:
  • hemolytic-uremic syndrome (@D59.3*-)
• Type 2 Excludes Notes:
  • von Willebrand disease (@D68.0*-)

Crosswalk Information

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This page was last updated on: 10/1/2023

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