Hermaphroditism, not elsewhere classified
ICD-10 Q56.0 is a billable code used to indicate a diagnosis of hermaphroditism, not elsewhere classified.
Hermaphroditism refers to a condition where an individual possesses both male and female reproductive organs or characteristics. This congenital condition can manifest in various forms, including ambiguous genitalia, where the external genitalia do not clearly resemble either male or female anatomy. In some cases, individuals may present with hypospadias, a condition where the urethral opening is located on the underside of the penis, or cryptorchidism, where one or both testes fail to descend into the scrotum. Uterine malformations may also be present, affecting the reproductive capabilities of individuals assigned female at birth. The diagnosis of hermaphroditism often involves a multidisciplinary approach, including genetic testing to identify chromosomal abnormalities that may contribute to the condition. Accurate coding is essential for appropriate management and treatment planning, as well as for understanding the underlying genetic factors that may influence the presentation of these congenital malformations.
Detailed physical examination findings, including descriptions of genitalia and any associated anomalies.
Evaluation of newborns with ambiguous genitalia, management of hypospadias or cryptorchidism in infants.
Consideration of psychosocial aspects and parental counseling regarding the child's condition.
Genetic testing results, family history of congenital conditions, and any chromosomal analysis performed.
Genetic counseling for families with a history of intersex conditions, interpretation of karyotype results.
Understanding the implications of genetic findings on treatment and management options.
Used for surgical correction of cryptorchidism in affected individuals.
Pre-operative assessment, surgical notes, and post-operative follow-up.
Pediatric urology may be involved in the surgical management.
Comprehensive documentation should include physical examination findings, genetic testing results, and any associated conditions. It is crucial to clearly describe the patient's genitalia and any anomalies present.
