ICD-10-CM QA0.0151 is the diagnosis code for FOXG1 syndrome. This code falls under the section "Genetic disorders, not elsewhere classified" within Chapter 17 — Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where QA0.0151 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, QA0.0151 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
QA0.0151 is the ICD-10-CM diagnosis code for "FOXG1 syndrome". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
The parent code of QA0.0151 is QA0.015 ("Neurodevelopmental disorders, related to genes associated with transcription and gene expression"). QA0.0151 provides a more specific classification within this category.
QA0.0151 is located in Section QA0 — "Genetic disorders, not elsewhere classified" within Chapter 17 of the ICD-10-CM Tabular List.
Use QA0.0151 when the patients documented diagnosis matches "FOXG1 syndrome" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for FOXG1 syndrome is QA0.0151.
Yes, QA0.0151 can be used as a primary diagnosis code since it is billable and specific.
QA0.0151 is in Chapter 17 of the ICD-10-CM Tabular List.
Yes, QA0.0151 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.