Familial adenomatous polyposis is a hereditary condition characterized by the development of numerous polyps in the colon and rectum, significantly increasing the risk of colorectal cancer. The condition is caused by mutations in the APC gene. Accurate coding with ICD-10 Code D13.91 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate surveillance and management.
ICD-10 Code D13.91 represents familial adenomatous polyposis, a genetic disorder leading to the formation of multiple adenomatous polyps in the gastrointestinal tract. This code should be used in clinical documentation and billing when diagnosing patients with this hereditary condition, which necessitates regular monitoring and potential surgical intervention to prevent colorectal cancer.
Familial adenomatous polyposis is primarily caused by mutations in the APC gene, leading to the development of hundreds to thousands of polyps in the colon, typically starting in adolescence or early adulthood. Without intervention, nearly all individuals with this condition will develop colorectal cancer by age 40. Early diagnosis and management are crucial to prevent malignancy.
ICD-10 Code D13.91 is utilized in SOAP notes to document the diagnosis of familial adenomatous polyposis, guiding clinical assessment and treatment planning. This code is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and facilitating appropriate management strategies.
In SOAP notes, ICD-10 Code D13.91 connects subjective patient reports and objective clinical findings to a formal diagnosis of familial adenomatous polyposis. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Familial adenomatous polyposis requires proactive management to prevent colorectal cancer. Treatment typically involves regular surveillance and may necessitate surgical intervention.


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Learn moreICD-10 Code D13.91 is critical in medical billing, particularly in hospital and outpatient settings, to ensure accurate reimbursement for services related to familial adenomatous polyposis.
| CPT Code | Description |
|---|---|
| 45378 | Colonoscopy, flexible, diagnostic, including collection of specimen(s) by brushing or washing. |
| 45380 | Colonoscopy, flexible, with biopsy, single or multiple. |
| 44140 | Colectomy, partial, with anastomosis. |
| 81201 | APC gene analysis, full gene sequence. |
Common Questions About Using ICD-10 Code D13.91 for Familial adenomatous polyposis
What are the main symptoms of familial adenomatous polyposis?
Symptoms of familial adenomatous polyposis may include the presence of multiple polyps in the colon, rectal bleeding, abdominal pain, and changes in bowel habits. Regular surveillance is crucial for early detection of colorectal cancer.
How is familial adenomatous polyposis diagnosed?
Diagnosis of familial adenomatous polyposis typically involves a combination of family history assessment, colonoscopy to identify polyps, and genetic testing for APC gene mutations.
What is the recommended management for familial adenomatous polyposis?
Management of familial adenomatous polyposis includes regular colonoscopic surveillance, potential prophylactic colectomy, and genetic counseling for affected individuals and their families.
How does ICD-10 Code D13.91 impact billing?
ICD-10 Code D13.91 is essential for accurate billing as it documents the diagnosis of familial adenomatous polyposis, ensuring that healthcare providers are reimbursed for surveillance and treatment services.
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