Glanzmann thrombasthenia
Billable / specificNew in FY2027
D69.11 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Glanzmann's disease
- Thromboasthenia (hemorrhagic) (hereditary)
Excludes1
Not coded here — never report together with this code.
- hemolytic-uremic syndrome (D59.3-) (from D69.1)
- benign hypergammaglobulinemic purpura (D89.0) (from D69)
- cryoglobulinemic purpura (D89.1) (from D69)
- essential (hemorrhagic) thrombocythemia (D47.3) (from D69)
- hemorrhagic thrombocythemia (D47.3) (from D69)
- purpura fulminans (D65) (from D69)
- thrombotic thrombocytopenic purpura (M31.19) (from D69)
- Waldenström hypergammaglobulinemic purpura (D89.0) (from D69)
Excludes2
Not included here — may be reported together when both conditions exist.
- von Willebrand disease (D68.0-) (from D69.1)
- autoimmune disease (systemic) NOS (M35.9) (from D69)
- certain conditions originating in the perinatal period (P00-P96) (from D69)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D69)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D69)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D69)
- human immunodeficiency virus [HIV] disease (B20) (from D69)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D69)
- neoplasms (C00-D49) (from D69)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D69)
Also known as
- Glanzmann's disease
- Thromboasthenia (hemorrhagic) (hereditary)
- Disease, diseased, Glanzmann's
- Disease, diseased, Naegeli's, meaning Glanzmann-Naegeli disease or thrombasthenia
- Glanzmanndisease or thrombasthenia
- Thrombasthenia
- Thromboasthenia
- Thrombocytasthenia
Parent code
- D69.1Qualitative platelet defectsHeader
Related codes
- D69.19Other qualitative platelet defectsBillable