Hereditary ataxia G11-

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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
  • 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...
  • 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)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan's syndrome (Q87.4)
    • 5-alpha-reductase deficiency (E29.1)
    Type 2 Excludes
    • Ehlers-Danlos syndromes (Q79.6-)
    • 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...
  • G11 Hereditary ataxia
    • G11.0 Congenital nonprogressive ataxia
    • G11.1 Early-onset cerebellar ataxia
      • G11.10 …… unspecified
      • G11.11 Friedreich ataxia
      • G11.19 Other 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