Other early-onset cerebellar ataxia
Billable / specificHCC V28 200
G11.19 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- 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
Excludes2
Not included here — may be reported together when both conditions exist.
- certain conditions originating in the perinatal period (P04-P96) (from G11)
- certain infectious and parasitic diseases (A00-B99) (from G11)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from G11)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99) (from G11)
- endocrine, nutritional and metabolic diseases (E00-E88) (from G11)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from G11)
- neoplasms (C00-D49) (from G11)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from G11)
- cerebral palsy (G80.-) (from G11)
- hereditary and idiopathic neuropathy (G60.-) (from G11)
- metabolic disorders (E70-E88) (from G11)
Also known as
- 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
- Ataxia, ataxy, ataxic, cerebellar, with essential tremor
- Ataxia, ataxy, ataxic, cerebellar, with myoclonus [Hunt's ataxia]
- Ataxia, ataxy, ataxic, cerebellar, with retained tendon reflexes
- Ataxia, ataxy, ataxic, Hunt's
- Ataxia, ataxy, ataxic, spinocerebellar, X-linked recessive
- Disease, diseased, Hunt's, dyssynergia cerebellaris myoclonica
- Dyssynergia, cerebellaris myoclonica
- Hunt's, disease or syndrome, dyssynergia cerebellaris myoclonica
- Ramsay-Hunt disease or syndrome, meaning dyssynergia cerebellaris myoclonica
- Syndrome, Hunt's, dyssynergia cerebellaris myoclonica
Parent code
- G11.1Early-onset cerebellar ataxiaHeader