D69.11 — Glanzmann thrombasthenia
Is D69.11 billable?
Yes — D69.11 is billable for FY2027. D69.11 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. D69.11 may be submitted for encounters from October 1, 2026 through September 30, 2027. D69.11 is new in FY2027.
D69.11 at a glance
| Code | D69.11 |
|---|---|
| Description | Glanzmann thrombasthenia |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
| FY2027 change | New in FY2027 |
Which MS-DRGs does D69.11 group to?
D69.11 sits in MDC 16 and helps define the logic of 1 MS-DRG (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 813Coagulation Disordersmedical
How is D69.11 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to D69.11. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Glanzmanndisease or thrombasthenia (-Naegeli)
- Thrombasthenia (Glanzmann) (hemorrhagic) (hereditary)
- Thromboasthenia (Glanzmann) (hemorrhagic) (hereditary)
- Thrombocytasthenia (Glanzmann)
- Disease, diseased › Glanzmann's
- Disease, diseased › Naegeli's › meaning Glanzmann-Naegeli disease or thrombasthenia
Inclusion terms
Alternative wording in documentation that is classified to D69.11.
- Glanzmann's disease
- Thromboasthenia (hemorrhagic) (hereditary)
Excludes1 — never code together — inherited from D69
The conditions below can never be reported together with D69.11 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Excludes1 — never code together — inherited from D69.1
The conditions below can never be reported together with D69.11 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
- hemolytic-uremic syndrome (D59.3-)
Excludes2 — not included here — inherited from Chapter 3
The conditions below are not part of D69.11, but a patient may have both at the same time. When documentation supports it, D69.11 and the excluded code may both 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)
Excludes2 — not included here — inherited from D69.1
The conditions below are not part of D69.11, but a patient may have both at the same time. When documentation supports it, D69.11 and the excluded code may both be reported.
- von Willebrand disease (D68.0-)