G11.2
BillableLate-onset cerebellar ataxia
Late-onset cerebellar ataxia
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- 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)
- cerebral palsy (G80.-)
- hereditary and idiopathic neuropathy (G60.-)
- metabolic disorders (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Hereditary cerebellar ataxia46808003
- Marie cerebellar ataxia46808003
- Marie's cerebellar ataxia46808003
- Azorean disease91952008
- MJD - Machado-Joseph disease91952008
- Machado Joseph disease91952008
- Machado-Joseph disease91952008
- Portuguese-Azorean disease91952008
- Spinocerebellar ataxia type 391952008
- Azorean disease, type I91953003
- Azorean disease, type II91954009
- Azorean disease, type III91955005
- Azorean disease, type IV91956006
- Late onset cerebellar ataxia230232005
- Progressive cerebellar ataxia230233000
- Periodic ataxia230234006
- Progressive spinocerebellar ataxia with decreased tendon reflexes230237004
- Progressive cerebellar ataxia with palatal myoclonus230239001
- Gordon Holmes syndrome230240004
- Luteinising hormone-releasing hormone deficiency with ataxia230240004
- Luteinizing hormone-releasing hormone deficiency with ataxia230240004
- Progressive cerebellar ataxia with hypogonadism230240004
- Episodic ataxia421455009
- Idiopathic late-onset cerebellar ataxia734023003
- Sporadic adult-onset ataxia of unknown aetiology734023003
- Sporadic adult-onset ataxia of unknown etiology734023003
- Sporadic adult-onset ataxia of unknown origin734023003
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome783060009
- Autosomal recessive spinocerebellar ataxia type 11783060009
- Adult-onset autosomal recessive cerebellar ataxia785302009
- Autosomal recessive spinocerebellar ataxia type 10785302009
- SCAR10 - autosomal recessive spinocerebellar ataxia type 10785302009
- SCA46 - spinocerebellar ataxia type 461279839002
- Spinocerebellar ataxia type 461279839002
- SCA45 - spinocerebellar ataxia type 451279840000
- Spinocerebellar ataxia type 451279840000
- Adult-onset SCA47 (spinocerebellar ataxia type 47)1303280001
- Adult-onset spinocerebellar ataxia type 471303280001
- PUM1-related cerebellar ataxia1303280001
- Pumilio RNA binding family member 1-related cerebellar ataxia1303280001
- Hereditary cerebellar atrophy431641000124107
Frequently Asked Questions
What is ICD-10 code G11.2?
ICD-10-CM code G11.2 represents "Late-onset cerebellar ataxia". It is a billable/specific code that can be used on a claim.
Is G11.2 a billable code?
Yes, G11.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.2 in?
G11.2 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.2 map to?
G11.2 maps to 20 SNOMED CT concepts: 1303280001, 785302009, 783060009, 91952008, 91953003, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.2?
G11.2 is linked to 1 UMLS Concept Unique Identifier: C0393524. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.