Hereditary ataxia - G11

Excludes2: This note means that the conditions described by two codes are not usually associated with each other but can sometimes occur together.

Type 2 Excludes:

cerebral palsy (G80.-)
hereditary and idiopathic neuropathy (G60.-)
metabolic disorders (E70-E88)

These ranges represents subcategories of Hereditary ataxia. The "G11" signifies that these are the diseases within this broad category.

Codes:

G11.0 - Congenital nonprogressive ataxia
G11.1 - Early-onset cerebellar ataxia
G11.10 - Early-onset cerebellar ataxia, 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
G11.5 - Hypomyelination - hypogonadotropic hypogonadism - hypodontia
G11.6 - Leukodystrophy with vanishing white matter disease
G11.8 - Other hereditary ataxias
G11.9 - Hereditary ataxia, unspecified