QA0.012 — Neurodevelopmental disorders, related to pathogenic variants in other receptor genes
Is QA0.012 billable?
Yes — QA0.012 is billable for FY2027. QA0.012 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. QA0.012 may be submitted for encounters from October 1, 2026 through September 30, 2027.
QA0.012 at a glance
| Code | QA0.012 |
|---|---|
| Description | Neurodevelopmental disorders, related to pathogenic variants in other receptor genes |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does QA0.012 group to?
QA0.012 sits in MDC 08 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 564Other Musculoskeletal System and Connective Tissue Diagnoses with MCCmedical
- 565Other Musculoskeletal System and Connective Tissue Diagnoses with CCmedical
- 566Other Musculoskeletal System and Connective Tissue Diagnoses without CC/MCCmedical
As a secondary diagnosis, QA0.012 is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.
How is QA0.012 listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to QA0.012. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Disorder › neurodevelopmental › other › receptor gene related (of)
Excludes2 — not included here — inherited from Chapter 17
The conditions below are not part of QA0.012, but a patient may have both at the same time. When documentation supports it, QA0.012 and the excluded code may both be reported.
- inborn errors of metabolism (E70-E88)
Code also — inherited from QA0
Two codes may be needed to describe the condition fully. Whether QA0.012 is sequenced first depends on the reason for the encounter.
How long has QA0.012 existed?
QA0.012 first appears in FY2026.
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.
What other codes are in the QA0.01 family? (5)
- QA0.010Neurodevelopmental disorders, related to pathogenic variants in ion channel genesnot billable
- QA0.011Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes
- QA0.013Neurodevelopmental disorders, related to pathogenic variants in other transporter and solute carrier genesnot billable
- QA0.014Neurodevelopmental disorders, related to pathogenic variants in synapse related genesnot billable
- QA0.015Neurodevelopmental disorders, related to genes associated with transcription and gene expressionnot billable