Turner's syndrome
Chapter 17:Congenital malformations and chromosomal abnormalities
ICD-10 Q96 is a used to indicate a diagnosis of turner's syndrome.
Turner's syndrome, classified under ICD-10 code Q96, is a chromosomal condition that affects females, characterized by the partial or complete absence of one of the two X chromosomes. This genetic disorder leads to a variety of developmental and physical features, including short stature, delayed puberty, and infertility. Individuals with Turner's syndrome may also exhibit other health issues such as heart defects, kidney abnormalities, and hearing problems. The clinical significance of this condition lies in its multifaceted impact on the patient's health and development, necessitating a comprehensive approach to management and care.
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
Q96 encompasses Turner's syndrome and its related manifestations, including short stature, ovarian insufficiency, and various congenital anomalies.
Q96 codes should be used when diagnosing Turner's syndrome or when documenting related health issues that stem from this genetic condition.
Documentation should include genetic testing results, clinical findings, and any associated health conditions to support the diagnosis of Turner's syndrome.