2025 ICD-10-CM code Q85.02
(Active) Effective Date: N/A Revision Date: N/A Deletion Date: N/A Congenital malformations - Phakomatoses, not elsewhere classified Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) Feed
Neurofibromatosis, type 2; Acoustic neurofibromatosis.
Medical necessity for coding Q85.02 is established by the presence of clinical findings or genetic confirmation consistent with Neurofibromatosis type 2.Management may include surgical intervention, radiation therapy, and/or monitoring for tumor growth.
Diagnosis and management of neurofibromatosis type 2, including genetic counseling, tumor surveillance, and treatment of associated symptoms.
- Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- Q85.0 - Neurofibromatosis (nonmalignant)
In simple words: Q85.02 is a code for a rare inherited condition called Neurofibromatosis type 2.This condition causes non-cancerous tumors to grow on the nerves in the head and spine.
Q85.02 is an ICD-10-CM code that classifies Neurofibromatosis, type 2, also known as acoustic neurofibromatosis.This is a genetic disorder characterized by the development of benign tumors on cranial and spinal nerves. It is less common than Neurofibromatosis type 1.
Example 1: A 25-year-old patient presents with progressive hearing loss and tinnitus. Imaging reveals bilateral vestibular schwannomas, consistent with Neurofibromatosis type 2. Code Q85.02 is used to document the diagnosis., A 40-year-old patient with a known diagnosis of Neurofibromatosis type 2 undergoes surgical resection of a spinal nerve schwannoma. Code Q85.02 is used to document the underlying condition., A 30-year-old patient with a family history of Neurofibromatosis type 2 undergoes genetic testing, confirming the diagnosis. Code Q85.02 is used to document the diagnosis even in the absence of overt symptoms.
Detailed family history of Neurofibromatosis type 2; imaging studies (MRI, CT) demonstrating characteristic tumors; genetic testing results (if performed).
** This code is specific to Neurofibromatosis type 2 and should not be used for other types of neurofibromatosis or related conditions.Always ensure accurate and comprehensive documentation to support the use of this code.
- Payment Status: Active
- Specialties:Neurology, Neurosurgery, Genetics, Otolaryngology
- Place of Service:Office, Hospital (Inpatient and Outpatient), Ambulatory Surgical Center