G11.1

Early-onset cerebellar ataxia

Non-billable header

G11.1 is a non-billable header code. Use one of the more specific codes below.

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)

Parent code

  • G11Hereditary ataxiaHeader

More specific codes G11.1

  • G11.10Early-onset cerebellar ataxia, unspecifiedBillable
  • G11.11Friedreich ataxiaBillable
  • G11.19Other early-onset cerebellar ataxiaBillable

Related codes

  • G11.0Congenital nonprogressive ataxiaBillable
  • G11.2Late-onset cerebellar ataxiaBillable
  • G11.3Cerebellar ataxia with defective DNA repairBillable
  • G11.4Hereditary spastic paraplegiaBillable
  • G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontiaBillable
  • G11.6Leukodystrophy with vanishing white matter diseaseBillable
  • G11.8Other hereditary ataxiasBillable
  • G11.9Hereditary ataxia, unspecifiedBillable

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