ICD-10-CM Codes
G00-G99 Diseases of the nervous system
G10-G14 Systemic atrophies primarily affecting the central nervous system

Hereditary ataxia G11- >

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...
)

Codes

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

Hereditary ataxia G11- >

Metabolic disorders