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D69.1

Qualitative platelet defects

Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 18 never code together
D69code
Excludes1
  • benign hypergammaglobulinemic purpura (D89.0)D89.0
  • cryoglobulinemic purpura (D89.1)D89.1
  • essential (hemorrhagic) thrombocythemia (D47.3)D47.3
  • hemorrhagic thrombocythemia (D47.3)D47.3
  • purpura fulminans (D65)D65
  • thrombotic thrombocytopenic purpura (M31.19)M31.19
  • Waldenström hypergammaglobulinemic purpura (D89.0)D89.0
D69.1code
Excludes1
Excludes2
D50-D89chapter
Excludes2
  • autoimmune disease (systemic) NOS (M35.9)M35.9
  • certain conditions originating in the perinatal period (P00-P96)P00-P96
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
  • endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
  • human immunodeficiency virus [HIV] disease (B20)B20
  • injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
  • neoplasms (C00-D49)C00-D49
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94

Excludes1 — never code together. The excluded condition and this one are mutually exclusive.

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes 5
D69.1code
Inclusion terms
  • Bernard-Soulier [giant platelet] syndrome
  • Glanzmann's disease
  • Grey platelet syndrome
  • Thromboasthenia (hemorrhagic) (hereditary)
  • Thrombocytopathy
Index entries leading here 14
  • Bernard-Soulier disease or thrombopathia D69.1
  • Disease, diseased — see also Syndrome
    • Bernard-Soulier (thrombopathy) D69.1
    • Glanzmann's (hereditary hemorrhagic thrombasthenia) D69.1
    • Naegeli's D69.1
  • Defect, defective Q89.9
    • platelets, qualitative D69.1
  • Deficiency, deficient
  • Diacyclothrombopathia D69.1
  • Disorder (of) — see also Disease
  • Dysfunction
  • Syndrome — see also Disease
    • giant platelet (Bernard-Soulier) D69.1
    • gray or grey (newborn) P93.0
  • Glanzmann (-Naegeli) disease or thrombasthenia D69.1
  • Thrombasthenia (Glanzmann) (hemorrhagic) (hereditary) D69.1
  • Thromboasthenia (Glanzmann) (hemorrhagic) (hereditary) D69.1
  • Thrombocytasthenia (Glanzmann) D69.1
  • Thrombocytopathy (dystrophic) (granulopenic) D69.1
  • Thrombopathy (Bernard-Soulier) D69.1
Alongside this code 8 same parent — D69
Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

CMS22HCC48 CMS28HCC112 ESRD21HCC48 ESRD24HCC48

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This code

Billable
yes
Code set
FY2026
Parent
D69
Block
D65-D69
Siblings
8

Present FY2024–FY2027.