Genetic carrier of other disease
ICD-10 Z14.8 is a billable code used to indicate a diagnosis of genetic carrier of other disease.
Z14.8 is used to indicate that an individual is a genetic carrier of a disease not classified elsewhere in the ICD-10 coding system. This code is significant in preventive care as it highlights the need for genetic counseling and potential screening for at-risk family members. Social determinants of health, such as socioeconomic status, education, and access to healthcare, can influence the management of genetic conditions. Preventive measures may include genetic testing and counseling, which can help inform family planning and early interventions. Screening for related conditions may also be warranted based on the specific genetic carrier status. Aftercare may involve regular monitoring and support for the individual and their family, addressing both medical and psychosocial needs.
Documentation should include family history, results of genetic tests, and any referrals for genetic counseling.
Routine checkups where genetic carrier status is discussed, screenings for related conditions, and aftercare follow-ups.
Consideration of social determinants such as access to genetic counseling services and education about genetic risks.
Documentation should include population-level data on genetic conditions and surveillance of carrier status in communities.
Epidemiological studies assessing the prevalence of genetic carriers and preventive health initiatives.
Focus on health disparities and access to genetic testing in underserved populations.
Used when a patient is tested for a specific genetic condition.
Documentation of the reason for testing and results.
Primary care providers should ensure that patients understand the implications of testing.
Z14.8 should be used when a patient is identified as a genetic carrier of a disease not classified elsewhere, and it is important to document the need for genetic counseling and any related preventive measures.
