G11.1 — Early-onset cerebellar ataxia
Is G11.1 billable?
No — G11.1 is a non-billable header code. G11.1 groups more specific codes and cannot be submitted on a claim. A valid ICD-10-CM code must be reported at the highest level of specificity available in its branch. Select one of the 3 billable codes beneath G11.1.
Billable codes under this header
G11.1 at a glance
| Code | G11.1 |
|---|---|
| Description | Early-onset cerebellar ataxia |
| Billable | No — header code |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Excludes2 — not included here — inherited from Chapter 6
The conditions below are not part of G11.1, but a patient may have both at the same time. When documentation supports it, G11.1 and the excluded code may both be reported.
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Excludes2 — not included here — inherited from G11
The conditions below are not part of G11.1, but a patient may have both at the same time. When documentation supports it, G11.1 and the excluded code may both be reported.
What codes fall under G11.1? (3)
How long has G11.1 existed?
G11.1 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.
- FY2021: G11.1 stopped being billable
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 G11 family? (8)
- G11.0Congenital nonprogressive ataxia
- G11.2Late-onset cerebellar ataxia
- G11.3Cerebellar ataxia with defective DNA repair
- G11.4Hereditary spastic paraplegia
- G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6Leukodystrophy with vanishing white matter disease
- G11.8Other hereditary ataxias
- G11.9Hereditary ataxia, unspecified