Short answer · Medically reviewed summary · Last updated: 2026-04-07

The ICD-10-CM code for Waldenstrom Macroglobulinemia is C88.0, while the historical ICD-9-CM code is 273.3. As a specialist who has worked with many patients navigating the complexities of Waldenstrom Macroglobulinemia, I know that understanding these diagnostic codes is often the first step in managing your medical records, insurance claims, and communication with your care team. Waldenstrom Macroglobulinemia is a rare, slow-growing type of B-cell lymphoma characterized by the overproduction of monoclonal immunoglobulin M (IgM) proteins.

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ICD10 code of Waldenstrom Macroglobulinemia and ICD9 code

ICD-10 and ICD-9 codes for Waldenstrom Macroglobulinemia, with classification details for clinicians, coders and patients.

ICD9 and ICD10 codes of Waldenstrom Macroglobulinemia

The ICD-10-CM code for Waldenstrom Macroglobulinemia is C88.0, while the historical ICD-9-CM code is 273.3.



As a specialist who has worked with many patients navigating the complexities of Waldenstrom Macroglobulinemia, I know that understanding these diagnostic codes is often the first step in managing your medical records, insurance claims, and communication with your care team. Waldenstrom Macroglobulinemia is a rare, slow-growing type of B-cell lymphoma characterized by the overproduction of monoclonal immunoglobulin M (IgM) proteins. Because it is a systemic lymphoplasmacytic lymphoma, precise classification is essential for ensuring that your treatment plan aligns with the latest clinical guidelines.



Why Classification Matters


While the ICD-10 code C88.0 is used universally for administrative purposes, the clinical reality of Waldenstrom Macroglobulinemia is far more nuanced. Because this condition can cause hyperviscosity syndrome—where the blood becomes too thick due to high levels of IgM protein—accurate coding helps your medical team justify the need for specific interventions like plasmapheresis or targeted therapy. When you are speaking with your insurance provider or coordinating care between specialists, referencing these codes can help streamline the approval of necessary diagnostic tests, such as bone marrow biopsies or specialized flow cytometry.



Navigating Your Care


Receiving a diagnosis of Waldenstrom Macroglobulinemia can feel overwhelming, and the administrative side of medical care often adds to that stress. Please remember that these codes are merely tools for the healthcare system; they do not define your journey or your prognosis. Many of our patients find comfort in knowing that because this is a recognized, distinct diagnosis, there is a clear pathway for clinical documentation. If you find your records are coded differently, do not hesitate to ask your hematologist-oncologist to verify that your chart reflects the C88.0 classification, as this is the standard identifier for Waldenstrom Macroglobulinemia within the international medical community.



Medical Disclaimer: This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your medical condition.



References



  • Orphanet: Waldenstrom Macroglobulinemia (ORPHA:527)

  • NIH Genetic and Rare Diseases Information Center (GARD): Waldenstrom Macroglobulinemia

  • International Waldenstrom's Macroglobulinemia Foundation (IWMF)

Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2026-04-07
Medical disclaimer: This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source: DiseaseMaps.org
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DECEMBER 22, 2015 - I was diagnosed in March 2007 at age 55 after a routine blood test showed anemia, and follow-up tests found hyperviscosity syndrome. IgM was 62, which is 6200 in US units. Hematologist said I would need treatment in a matter of mo...
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    I was dxed with MGUS in 2008 by a nephrologist that I was referred to because of an e-GFR result. I progressed to Waldenstroms in 2014 after investigating my PN at MAYO. My PN is Anti-MAG. I was treated with Rituxan in January of 2015. I have...
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_I WAS DIAGNOSED  NEARLY 3 YEARS AGO WHEN A BLOOD TEST FOR SOMETHING ELSE SHOWED A HIGH IGM.  HAD 2 ROUNDS OF CHEMO (VELCADE) AND HAD SOME BAD SIDE EFFECTS.  AFTER A SECOND OPINION AT THE JAMES CANCER CENTER IN COLUMBUS, OHIO  IT WAS DETERMINED I...
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spring 2014 sudden weight loss (2 stone) anaemic night sweats waekness; doctors went down gastric route until heart started to fail: superb consultant asked for tests in jan 15; even then had to spend a few months learning i had kidney cancer. in ...
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My husband was diagnosed with WM in mid 2014. He has been in the watchful waiting mode. At his last onc appointment he has been told he needs to start treatment. He has been trying to heal his body with nutrition and supplements and is terrified of c...

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