2027 ICD-10-CM Diagnosis Code D69.19Other qualitative platelet defects
D69.19 is a billable ICD-10-CM diagnosis code for other qualitative platelet defects. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 813.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Abnormal platelet destruction
- Abnormal platelet production
- Acquired PF-3 disease
- Acquired platelet disorder
- Acquired platelet function disorder
- Acquired storage pool deficiency
- Autoimmune state
- Autoplatelet sensitivity
- Autosensitivity
- Bernard Soulier syndrome
- Bleeding diathesis due to collagen receptor defect
- Congenital dyserythropoietic anemia
- Cyclooxygenase deficiency
- Decreased platelet destruction
- Decreased platelet life span
- 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
- 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
- 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 caused by aspirin
- Platelet membrane defect
- 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
- Thromboxane generation defect
- Thromboxane synthetase deficiency
- White platelet syndrome
- X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
Instructional NotesGuidance
Instructions from the official ICD-10-CM Tabular List that apply to D69.19: its own notes plus those printed at D69.1, D69, and Chapter 3. A note printed at a category, block or chapter applies to every code under it.
Applicable To
Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.
- Bernard-Soulier [giant platelet] syndrome
- Grey platelet syndrome
- Thrombocytopathy
Excludes1
Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.
Excludes2
Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Source: CMS ICD-10-CM Tabular List. How to read instructional notes.
Referenced in Other NotesGuidance
Instructional notes printed at other codes that name D69.19, its category, or a range that includes it.
Excludes1 1
These codes carry an Excludes1 note naming D69.19: they are not reported together with it, unless the two conditions are unrelated.
Excludes2 1
These codes carry an Excludes2 note naming D69.19: its condition is not part of those codes, and both may be reported when the patient has both.
- Block R70-R79 Abnormal findings on examination of blood, without diagnosisabnormalities of platelets and thrombocytes (D69.-) names D69.-, which includes this code
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
Diacyclothrombopathia D69.19
Disease, diseased See Also: Syndrome;
Disorder (of) See Also: Disease;
platelets D69.19
platelets D69.19
Clinical InformationClinical
Blood Platelet Disorders
disorders caused by abnormalities in platelet count or function.
Code History & ChangesHistory
New Code D69.19 was added to the ICD-10-CM code set for FY 2027, effective October 1, 2026.
Replacement D69.19 replaces the following previously assigned code(s):
- D69.1 - Qualitative platelet defects
Questions About D69.19Overview
What is the ICD-10 code for other qualitative platelet defects?
The ICD-10-CM code for other qualitative platelet defects is D69.19 (sometimes written as D6919). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
Is D69.19 (Qualitative platelet defects) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other qualitative platelet defects on HIPAA-covered claims from October 1, 2026 through September 30, 2027.
What MS-DRG does D69.19 group to?
When other qualitative platelet defects is the principal diagnosis on an inpatient stay, it groups to MS-DRG 813 (coagulation Disorders), which carries a relative weight of 1.5279. Higher weights mean higher Medicare reimbursement.
Can D69.19 be reported with a code from D59.3?
Not as a rule. The Excludes1 note at D69.1, which applies to D69.19, lists "hemolytic-uremic syndrome (D59.3-)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).
