Genetic carrier
ICD-10 Z14 is a used to indicate a diagnosis of genetic carrier.
The ICD-10 Level 1 Category code Z14 pertains to individuals identified as genetic carriers of specific hereditary conditions. This category encompasses various genetic disorders, including but not limited to cystic fibrosis, sickle cell disease, and Tay-Sachs disease. Being a genetic carrier means that an individual possesses one copy of a mutated gene that could be passed on to offspring, potentially leading to genetic disorders in future generations. The clinical significance of identifying genetic carriers lies in the ability to provide genetic counseling, inform reproductive choices, and guide preventive healthcare measures for affected individuals and their families.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Z14 includes conditions such as cystic fibrosis, sickle cell disease, Tay-Sachs disease, and other hereditary genetic disorders where the individual is identified as a carrier.
Z14 codes should be used when a patient has been identified as a genetic carrier through testing, and it is important to document this status for clinical management and family planning.
Documentation should include genetic test results, family history indicating potential hereditary conditions, and any counseling provided regarding the implications of being a carrier.
