2026 ICD-10-CM Diagnosis Code QA0.8Other neurodevelopmental disorders related to pathogenic variants in other specific genes
QA0.8 is a billable ICD-10-CM diagnosis code for other neurodevelopmental disorders related to pathogenic variants in other specific genes. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 564 through 566. The code is exempt from POA reporting.
Code Identity
Code Classification
Present on Admission (POA)Billing
QA0.8 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Disorder (of) - See Also: Disease;
- specified NEC - F88
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Disorder(of)
- neurodevelopmental
- specified NEC
- related to pathogenic variants in specific genes NEC
Code History & ChangesHistory
New Code QA0.8 was added to the ICD-10-CM code set for FY 2026, effective October 1, 2025.
Replacement QA0.8 replaces the following previously assigned code(s):
- F89 - Unspecified disorder of psychological development
Questions About QA0.8Overview
Is QA0.8 a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other neurodevelopmental disorders related to pathogenic variants in other specific genes on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does QA0.8 group to?
When other neurodevelopmental disorders related to pathogenic variants in other specific genes is the principal diagnosis on an inpatient stay, it groups to MS-DRG 564, 565, 566, with relative weights from 0.7493 to 1.5436 depending on complications. Higher weights mean higher Medicare reimbursement.
Is QA0.8 exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for other neurodevelopmental disorders related to pathogenic variants in other specific genes on inpatient claims.
