D69.49
BillableOther primary thrombocytopenia
Other primary thrombocytopenia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Megakaryocytic hypoplasia
- Primary thrombocytopenia NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •benign hypergammaglobulinemic purpuraD89.0
- •cryoglobulinemic purpuraD89.1
- •essential (hemorrhagic) thrombocythemiaD47.3
- •hemorrhagic thrombocythemiaD47.3
- •purpura fulminansD65
- •thrombotic thrombocytopenic purpuraM31.19
- •Waldenström hypergammaglobulinemic purpuraD89.0
- •transient neonatal thrombocytopeniaP61.0
- •Wiskott-Aldrich syndromeD82.0
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(2)
Also Known As / Clinical Terms(66)
SNOMED CT
- Congenital cutaneous angiomatosis73716000
- Thrombocytopenia due to diminished platelet production78345002
- Thrombocytopenia due to defective platelet production82190001
- Haemangioma-haemorrhage syndrome86635005
- Haemangiomatosis with thrombocytopenia86635005
- Hemangioma-hemorrhage syndrome86635005
- Hemangiomatosis with thrombocytopenia86635005
- Kasabach Merritt syndrome86635005
- Kasabach-Merritt syndrome86635005
- Thrombocytopenia-haemangioma syndrome86635005
- Thrombocytopenia-hemangioma syndrome86635005
- Decreased megakaryocyte production103213002
- Amegakaryocytic thrombocytopenia234482009
- Megakaryocytic thrombocytopenia234483004
- Mediterranean thrombocytopenia234487003
- Primary thrombocytopenia267534000
- Thrombocytopenic purpura302873008
- Megakaryocytic aplasia359536009
- Megakaryocytic hypoplasia359536009
- Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome1222681008
- Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome1222681008
- Evans syndrome associated with primary immunodeficiency1222681008
- TPPII (tripeptidyl-peptidase II) deficiency1222681008
- TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease1222681008
- TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease1222681008
- Tripeptidyl-peptidase II deficiency1222681008
UMLS
- Megakaryocytic aplasiaC1260901
- Megakaryocytic aplasia (disorder)C1260901
- Megakaryocytic hypoplasiaC1260901
- Other Primary ThrombocytopeniaC0477317
- Other primary thrombocytopeniaC0477317
- Primary thrombocytopeniaC0701157
- Primary thrombocytopenia (disorder)C0701157
- Primary thrombocytopenia NOSC0701157
- primary thrombocytopeniaC0701157
- primary thrombocytopeniasC0701157
Clinical Terms
- TRIANGLE (TPPII-related immunodeficiency, autoimmunity, neurodevelopmental delay, impaired glycolysis, lysosomal expansion) disease
- Haemangiomatosis with thrombocytopenia
- Amegakaryocytic thrombocytopenia
- primary thrombocytopenia
- Primary thrombocytopenia (disorder)
- Thrombocytopenia due to diminished platelet production
- Thrombocytopenic purpura
- Hemangioma-hemorrhage syndrome
- Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
- Megakaryocytic hypoplasia
- Evans syndrome associated with primary immunodeficiency
- Megakaryocytic thrombocytopenia
- Kasabach-Merritt syndrome
- Kasabach Merritt syndrome
- Thrombocytopenia due to defective platelet production
- Thrombocytopenia-haemangioma syndrome
- Thrombocytopenia-hemangioma syndrome
- Autoimmune haemolytic anaemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome
- Haemangioma-haemorrhage syndrome
- TPPII-related immunodeficiency, autoimmunity and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease
- Congenital cutaneous angiomatosis
- Megakaryocytic aplasia (disorder)
- TPPII (tripeptidyl-peptidase II) deficiency
- Primary thrombocytopenia NOS
- primary thrombocytopenias
- Hemangiomatosis with thrombocytopenia
- Mediterranean thrombocytopenia
- Megakaryocytic aplasia
- Tripeptidyl-peptidase II deficiency
- Decreased megakaryocyte production
Frequently Asked Questions
What is the ICD-10 code for other primary thrombocytopenia?
The ICD-10-CM code for other primary thrombocytopenia is D69.49. The full clinical description is "Other primary thrombocytopenia". D69.49 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D69.49 mean?
ICD-10-CM code D69.49 represents “Other primary thrombocytopenia”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D69.49 a billable code?
Yes, D69.49 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D69.49 in?
D69.49 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D69.49?
D69.49 has Excludes1 notes indicating codes that cannot be used together with it, including: benign hypergammaglobulinemic purpura (D89.0); cryoglobulinemic purpura (D89.1); essential (hemorrhagic) thrombocythemia (D47.3); and 6 more.
What SNOMED CT codes does D69.49 map to?
D69.49 maps to 12 SNOMED CT concepts: 234482009, 1222681008, 73716000, 103213002, 86635005, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D69.49?
D69.49 is linked to 3 UMLS Concept Unique Identifiers: C1260901, C0477317, C0701157. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D69.49 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other primary thrombocytopenia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D69.49?
There is no direct ICD-11 mapping available for D69.49 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.