Home
NPI Lookup
ICD-10 Lookup
CLIA Lookup
NDC Lookup
HCPCS Lookup
Taxonomy Codes
G11.2 LATE-ONSET CEREBELLAR ATAXIA
Home
ICD-10 List
G00–G99
G10-G14
G11
G11.2
Code Information
Diagnosis Code:
G11.2
Short Description:
Late-onset cerebellar ataxia
Long Description:
Late-onset cerebellar ataxia
Code Version:
2025 ICD-10-CM
The code G11.2 is VALID for claim submission
Code Classification
Diseases of the nervous system (G00–G99)
Systemic atrophies primarily affecting the central nervous system (G10-G14)
Hereditary ataxia (G11)
This code is valid for
adult diagnoses
Synonyms
Adult-onset autosomal recessive cerebellar ataxia
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
Azorean disease
Azorean disease, type I
Azorean disease, type II
Azorean disease, type III
Azorean disease, type IV
Episodic ataxia
Hereditary cerebellar atrophy
Late onset cerebellar ataxia
Marie's cerebellar ataxia
Periodic ataxia
Progressive cerebellar ataxia
Progressive cerebellar ataxia with hypogonadism
Progressive cerebellar ataxia with palatal myoclonus
Progressive spinocerebellar ataxia with decreased tendon reflexes
PUM1-related cerebellar ataxia
Spinocerebellar ataxia type 45
Spinocerebellar ataxia type 46
Sporadic adult-onset ataxia of unknown etiology
Crosswalk Information
ICD-10 Code
ICD-9 Code
ICD-9 Description
G11.2
334.2
Primary cerebellar degen
This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.
Similar Codes
ICD-10 Code
ICD-10 Description
G11
Hereditary ataxia
G11.0
Congenital nonprogressive ataxia
G11.1
Early-onset cerebellar ataxia
G11.10
Early-onset cerebellar ataxia, unspecified
G11.11
Friedreich ataxia
G11.19
Other early-onset cerebellar ataxia
G11.3
Cerebellar ataxia with defective DNA repair
G11.4
Hereditary spastic paraplegia
G11.5
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
G11.6
Leukodystrophy with vanishing white matter disease
G11.8
Other hereditary ataxias
G11.9
Hereditary ataxia, unspecified
This page was last updated on: 10/1/2025
Previous Code
Next Code