2018/2019 ICD-10-CM Diagnosis Code G11

Hereditary ataxia

Type 2 Excludes
Type 2 Excludes Help
A type 2 excludes note represents "not included here". A type 2 excludes note indicates that the condition excluded is not part of the condition it is excluded from but a patient may have both conditions at the same time. When a type 2 excludes note appears under a code it is acceptable to use both the code (G11) and the excluded code together.
  • cerebral palsy (
    ICD-10-CM Diagnosis Code G80
    • G80 Cerebral palsy
      • G80.0 Spastic quadriplegic cerebral palsy
      • G80.1 Spastic diplegic cerebral palsy
      • G80.2 Spastic hemiplegic cerebral palsy
      • G80.3 Athetoid cerebral palsy
      • G80.4 Ataxic cerebral palsy
      • G80.8 Other cerebral palsy
      • G80.9 Cerebral palsy, unspecified
    G80.-
    )
  • hereditary and idiopathic neuropathy (
    ICD-10-CM Diagnosis Code G60
    • G60 Hereditary and idiopathic neuropathy
      • G60.0 Hereditary motor and sensory neuropathy
      • G60.1 Refsum's disease
      • G60.2 Neuropathy in association with hereditary ata...
      • G60.3 Idiopathic progressive neuropathy
      • G60.8 Other hereditary and idiopathic neuropathies
      • G60.9 Hereditary and idiopathic neuropathy, unspeci...
    G60.-
    )
  • metabolic disorders (E70-E88
    ICD-10-CM Range E70-E88

    Metabolic disorders

    Type 1 Excludes
    • androgen insensitivity syndrome (E34.5-)
    • congenital adrenal hyperplasia (E25.0)
    • Ehlers-Danlos syndrome (Q79.6)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan's syndrome (Q87.4)
    • 5-alpha-reductase deficiency (E29.1)
    • E70 Disorders of aromatic amino-acid metabol...
    • E71 Disorders of branched-chain amino-acid m...
    • E72 Other disorders of amino-acid metabolism
    • E73 Lactose intolerance
    • E74 Other disorders of carbohydrate metaboli...
    • E75 Disorders of sphingolipid metabolism and...
    • E76 Disorders of glycosaminoglycan metabolis...
    • E77 Disorders of glycoprotein metabolism
    • E78 Disorders of lipoprotein metabolism and ...
    • E79 Disorders of purine and pyrimidine metab...
    • E80 Disorders of porphyrin and bilirubin met...
    • E83 Disorders of mineral metabolism
    • E84 Cystic fibrosis
    • E85 Amyloidosis
    • E86 Volume depletion
    • E87 Other disorders of fluid, electrolyte an...
    • E88 Other and unspecified metabolic disorder...
    )
The following code(s) above G11 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to G11:
  • G00-G99
    2019 ICD-10-CM Range G00-G99

    Diseases of the nervous system

    Type 2 Excludes
    • 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)
    Diseases of the nervous system
Code History
Code annotations containing back-references to G11:
ICD-10-CM Codes Adjacent To G11
G05.3 Encephalitis and encephalomyelitis in diseases classified elsewhere
G05.4 Myelitis in diseases classified elsewhere
G06 Intracranial and intraspinal abscess and granuloma
G06.0 Intracranial abscess and granuloma
G06.1 Intraspinal abscess and granuloma
G06.2 Extradural and subdural abscess, unspecified
G07 Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
G08 Intracranial and intraspinal phlebitis and thrombophlebitis
G09 Sequelae of inflammatory diseases of central nervous system
G10 Huntington's disease
G11 Hereditary ataxia
G11.0 Congenital nonprogressive ataxia
G11.1 Early-onset cerebellar ataxia
G11.2 Late-onset cerebellar ataxia
G11.3 Cerebellar ataxia with defective DNA repair
G11.4 Hereditary spastic paraplegia
G11.8 Other hereditary ataxias
G11.9 Hereditary ataxia, unspecified
G12 Spinal muscular atrophy and related syndromes
G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
G12.1 Other inherited spinal muscular atrophy

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.