Genetic susceptibility to other disease
ICD-10 Z15.89 is a billable code used to indicate a diagnosis of genetic susceptibility to other disease.
Z15.89 indicates a genetic predisposition to diseases not specifically classified elsewhere. This code is crucial for identifying patients who may be at increased risk for certain conditions due to hereditary factors. Understanding genetic susceptibility is vital for preventive care, as it allows healthcare providers to tailor screening and intervention strategies based on individual risk profiles. Social determinants of health, such as socioeconomic status, access to healthcare, and education, can significantly influence the management of these patients. Preventive measures may include genetic counseling, lifestyle modifications, and regular screenings for diseases that the patient is genetically predisposed to. Aftercare may involve ongoing monitoring and support to mitigate risks associated with their genetic background, ensuring that patients receive comprehensive care that addresses both their medical and social needs.
Document family history, genetic testing results, and preventive care plans.
Routine checkups where genetic risk factors are assessed, screenings for predisposed conditions.
Consider social determinants such as access to genetic counseling and screening services.
Population health data on genetic predispositions and disease prevalence.
Epidemiological studies assessing the impact of genetic factors on public health outcomes.
Focus on health equity and access to preventive services for at-risk populations.
Used in conjunction with Z15.89 for patients with a family history of breast or ovarian cancer.
Documentation of family history and justification for genetic testing.
Primary care providers should coordinate with genetic counselors for comprehensive care.
Z15.89 should be used when a patient has a documented genetic predisposition to diseases but does not currently have the disease. It is essential to support this code with appropriate documentation of genetic testing and family history.