G11.19
BillableOther early-onset cerebellar ataxia
Other early-onset cerebellar ataxia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 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
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
- Vestibular ataxia22443004
- Vestibulocerebellar ataxia22443004
- Primary cerebellar degeneration23732000
- Dyssynergia cerebellaris progressiva41009006
- Progressive cerebellar tremor41009006
- Ramsay Hunt syndrome 141009006
- X chromosome-linked sideroblastic anaemia48983004
- X chromosome-linked sideroblastic anemia48983004
- X-linked sideroblastic anaemia48983004
- X-linked sideroblastic anemia48983004
- Dentate cerebellar ataxia73495003
- Dentato-rubral atrophy syndrome73495003
- Dyssynergia cerebellaris myoclonica73495003
- Hunt's disease73495003
- Early onset cerebellar ataxia with myoclonus192871008
- Ramsay Hunt syndrome - ataxia192871008
- EOCA - Early onset cerebellar ataxia with retained tendon reflexes230228004
- Early onset cerebellar ataxia with retained tendon reflexes230228004
- Early onset cerebellar ataxia with hypogonadism230229007
- Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy230230002
- Early onset cerebellar ataxia with essential tremor230231003
- Progressive spinocerebellar ataxia with retained tendon reflexes230238009
- X-linked intellectual disability with ataxia and apraxia syndrome718845002
- X-linked sideroblastic anaemia with spinocerebellar ataxia719816006
- X-linked sideroblastic anemia with spinocerebellar ataxia719816006
- X-linked ataxia deafness syndrome719817002
- X-linked spinocerebellar ataxia type 3719817002
- X-linked ataxia dementia syndrome719818007
- X-linked spinocerebellar ataxia type 4719818007
- Autosomal recessive posterior column ataxia and retinitis pigmentosa724065003
- Posterior column ataxia with retinitis pigmentosa syndrome724065003
- Infantile onset spinocerebellar ataxia724227000
- Ohaha syndrome724227000
- Ophthalmoplegia, hypotonia, ataxia, hypoacusis, athetosis syndrome724227000
- Autosomal recessive cerebellar ataxia, cognitive defect syndrome763351003
- Autosomal recessive spinocerebellar ataxia type 14763351003
- Spectrin-associated autosomal recessive cerebellar ataxia763351003
- Spectrin-associated autosomal recessive cerebellar ataxia type 1763351003
- Autosomal recessive spinocerebellar ataxia type 6785300001
- Infantile-onset autosomal recessive non progressive cerebellar ataxia785300001
- Infantile-onset autosomal recessive nonprogressive cerebellar ataxia785300001
- SCAR6 - autosomal recessive spinocerebellar ataxia type 6785300001
- Autosomal recessive spinocerebellar ataxia type 7785301002
- Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia785301002
- SCAR7 - autosomal recessive spinocerebellar ataxia type 7785301002
- Non-progressive cerebellar ataxia1119354003
UMLS
- Ataxia, harding typeC0393520
- CEREBELLAR ATAXIA, EARLY-ONSET, WITH RETAINED TENDON REFLEXESC0393520
- Cerebellar Ataxia, Early-Onset, with Retained Tendon ReflexesC0393520
- Cerebellar ataxia early onset with retained tendon reflexC0393520
- EOCAC0393520
- EOCA - Early onset cerebellar ataxia with retained tendon reflexesC0393520
- Early onset cerebellar ataxia with retained tendon reflexesC0393520
- Early onset cerebellar ataxia with retained tendon reflexes (disorder)C0393520
- Early-onset cerebellar ataxia with retained tendon reflexesC0393520
- Harding ataxiaC0393520
- Early onset cerebellar ataxia with essential tremorC0393523
- Early onset cerebellar ataxia with essential tremor (disorder)C0393523
- Early-onset cerebellar ataxia with essential tremorC0393523
- Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia]C5385211
- Other Early-Onset Cerebellar AtaxiaC5384686
- Other early-onset cerebellar ataxiaC5384686
- X-linked recessive spinocerebellar ataxiaC2875046
Frequently Asked Questions
What is the ICD-10 code for other early-onset cerebellar ataxia?
The ICD-10-CM code for other early-onset cerebellar ataxia is G11.19. The full clinical description is "Other early-onset cerebellar ataxia". G11.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G11.19 mean?
ICD-10-CM code G11.19 represents "Other early-onset cerebellar ataxia". It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G11.19 a billable code?
Yes, G11.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G11.19 in?
G11.19 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G11.19 map to?
G11.19 maps to 21 SNOMED CT concepts: 763351003, 724065003, 785300001, 785301002, 73495003, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G11.19?
G11.19 is linked to 5 UMLS Concept Unique Identifiers: C0393520, C0393523, C5385211, C5384686, C2875046. 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.