G11.19 - Other early-onset cerebellar ataxia
| ICD-10: | G11.19 |
| Short Description: | Other early-onset cerebellar ataxia |
| Long Description: | Other early-onset cerebellar ataxia |
| Status: | Valid for Submission |
| Version: | ICD-10-CM 2023 |
| Code Classification: |
G11.19 is a billable ICD-10 code used to specify a medical diagnosis of other early-onset cerebellar ataxia. The code is valid during the fiscal year 2023 from October 01, 2022 through September 30, 2023 for the submission of HIPAA-covered transactions.
Approximate Synonyms
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Autosomal recessive posterior column ataxia and retinitis pigmentosa
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia
- Dyssynergia cerebellaris myoclonica
- Early onset cerebellar ataxia with essential tremor
- Early onset cerebellar ataxia with hypogonadism
- Early onset cerebellar ataxia with myoclonus
- Early onset cerebellar ataxia with retained tendon reflexes
- Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy
- Infantile onset spinocerebellar ataxia
- Infantile-onset autosomal recessive non progressive cerebellar ataxia
- Primary cerebellar degeneration
- Progressive cerebellar tremor
- Progressive spinocerebellar ataxia with retained tendon reflexes
- Spectrin-associated autosomal recessive cerebellar ataxia
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 10
- Spinocerebellar ataxia type 12
- Spinocerebellar ataxia type 13
- Spinocerebellar ataxia type 15/16
- Spinocerebellar ataxia type 17
- Spinocerebellar ataxia type 18
- Spinocerebellar ataxia type 19
- Spinocerebellar ataxia type 2
- Spinocerebellar ataxia type 20
- Spinocerebellar ataxia type 21
- Spinocerebellar ataxia type 23
- Spinocerebellar ataxia type 25
- Spinocerebellar ataxia type 26
- Spinocerebellar ataxia type 27
- Spinocerebellar ataxia type 28
- Spinocerebellar ataxia type 29
- Spinocerebellar ataxia type 30
- Spinocerebellar ataxia type 31
- Spinocerebellar ataxia type 32
- Spinocerebellar ataxia type 36
- Spinocerebellar ataxia type 37
- Spinocerebellar ataxia type 4
- Spinocerebellar ataxia type 5
- Spinocerebellar ataxia type 6
- Spinocerebellar ataxia type 7
- Spinocerebellar ataxia type 8
- Vestibulocerebellar ataxia
- X chromosome-linked sideroblastic anemia
- X-linked intellectual disability with ataxia and apraxia syndrome
- X-linked sideroblastic anemia with spinocerebellar ataxia
- X-linked spinocerebellar ataxia type 3
- X-linked spinocerebellar ataxia type 4
Clinical Information
- Spinocerebellar Ataxia Type 7-. an autosomal dominant inherited neurodegenerative disorder caused by mutations in the atxn7 gene. it is characterized by progressive cerebellar ataxia, including dysarthria and dysphagia, cone-rod and retinal dystrophy, and progressive central visual loss resulting in blindness.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to this diagnosis code:
Inclusion Terms
Inclusion TermsThese terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Early-onset cerebellar ataxia with essential tremor
- Early-onset cerebellar ataxia with myoclonus Hunt's ataxia
- Early-onset cerebellar ataxia with retained tendon reflexes
- X-linked recessive spinocerebellar ataxia
Index to Diseases and Injuries References
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for this diagnosis code are found in the injuries and diseases index:
- - Ataxia, ataxy, ataxic - R27.0
- - cerebellar (hereditary) - G11.9
- - with
- - essential tremor - G11.19
- - myoclonus [Hunt's ataxia] - G11.19
- - retained tendon reflexes - G11.19
- - with
- - Hunt's - G11.19
- - spinocerebellar, X-linked recessive - G11.19
- - cerebellar (hereditary) - G11.9
- - Dyssynergia
- - cerebellaris myoclonica (Hunt's ataxia) - G11.19
- - Hunt's
- - Ramsay-Hunt disease or syndrome - See Also: Hunt's disease; - B02.21
- - meaning dyssynergia cerebellaris myoclonica - G11.19
Replacement Code
G1119 replaces the following previously assigned ICD-10 code(s):
- G11.1 - Early-onset cerebellar ataxia
Code History
- FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
- FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
- FY 2021 - Code Added, effective from 10/1/2020 through 9/30/2021