D69.1 Qualitative platelet defects

Billable ICD-10-CM code, FY2026.

Applicable to

• Bernard-Soulier [giant platelet] syndrome
• Glanzmann's disease
• Grey platelet syndrome
• Thromboasthenia (hemorrhagic) (hereditary)
• Thrombocytopathy

Excludes1 (never code together)

• hemolytic-uremic syndrome (D59.3-)

Excludes2 (not included here)

• von Willebrand disease (D68.0-)

Applies from D69 Purpura and other hemorrhagic conditions

Excludes1 (never code together)

• benign hypergammaglobulinemic purpura (D89.0)
• cryoglobulinemic purpura (D89.1)
• essential (hemorrhagic) thrombocythemia (D47.3)
• hemorrhagic thrombocythemia (D47.3)
• purpura fulminans (D65)
• thrombotic thrombocytopenic purpura (M31.19)
• Waldenström hypergammaglobulinemic purpura (D89.0)

Risk adjustment (HCC)

• CMS-HCC V28: HCC 112 — Immune Thrombocytopenia and Specified Coagulation Defects and Hemorrhagic Conditions
• CMS-HCC V22: HCC 48 — Coagulation Defects and Other Specified Hematological Disorders
• ESRD V24: HCC 48

MS-DRG index

Defines the logic of DRG(s) 813 in MDC 16.

Approximate ICD-9-CM (GEMs)

• 287.1 Qualitative platelet defects

Code annotations containing back-references to D69.1

Back-references to D69.1

• Code Also: D68.09 Other von Willebrand disease (", if applicable, qualitative platelet defects (D69.1)")

Back-references to D69

• Type 1 Excludes: R23.3 Spontaneous ecchymoses ("purpura (D69.-)")

Diagnosis Index entries for D69.1

• Bernard-Soulier disease or thrombopathia
• Defect, defective › platelets, qualitative
• Deficiency, deficient › platelet NEC
• Diacyclothrombopathia
• Disease, diseased › Bernard-Soulier (thrombopathy)
• Disease, diseased › Glanzmann's (hereditary hemorrhagic thrombasthenia)
• Disease, diseased › Naegeli's
• Disorder (of) › platelets
• Dysfunction › platelets
• Glanzmann (-Naegeli) disease or thrombasthenia
• Syndrome › giant platelet (Bernard-Soulier)
• Syndrome › gray or grey (newborn) › platelet
• Thrombasthenia (Glanzmann) (hemorrhagic) (hereditary)
• Thromboasthenia (Glanzmann) (hemorrhagic) (hereditary)
• Thrombocytasthenia (Glanzmann)
• Thrombocytopathy (dystrophic) (granulopenic)
• Thrombopathy (Bernard-Soulier)

Nearby codes

• D69 Purpura and other hemorrhagic conditions
• D69.0 Allergic purpura
• D69.1 Qualitative platelet defects (this code)
• D69.2 Other nonthrombocytopenic purpura
• D69.3 Immune thrombocytopenic purpura
• D69.4 Other primary thrombocytopenia
• D69.41 Evans syndrome
• D69.42 Congenital and hereditary thrombocytopenia purpura