Q85.82
BillableOther Cowden syndrome
Q85.82 is the ICD-10-CM code for Other Cowden syndrome. It is a billable, specific code valid for reimbursement.
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
What this means — in plain language
MedlinePlus · NIHCowden syndrome is a genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain cancers. Almost everyone with Cowden syndrome develops hamartomas. These growths are most commonly found on the skin and mucous membranes (such as the lining of the mouth and nose), but they can also occur in the intestine and other parts of the body. The…
Read more about Cowden syndrome at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Medications indicated for this condition
FDA labeling- Interferon Gamma-1bInterferon gamma [EPC]›
- MirdametinibKinase Inhibitor [EPC]›
- SelumetinibKinase Inhibitor [EPC]›
Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.
Conditions mapped to this code
MedlinePlus · NIHPlain-language health-topic references grounded in MedlinePlus (NIH/NLM).
Frequently asked questions
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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