ICD 10 CM Codes

G11.1 Early-onset cerebellar ataxia
Non-Billable CodeG11.1 is not a billable ICD-10-CM diagnosis code and cannot be used to indicate a medical diagnosis.
Type 2 Excludes
cerebral palsy (G80.-)
hereditary and idiopathic neuropathy (G60.-)
metabolic disorders (E70-E88)
ICD-10-CM Index Entry
ICD-10-CM Index entries containing back-references to ICD-10-CM '.G11.1.'
Ataxia, ataxy, ataxic; cerebellar (hereditary); early-onset
Ataxia, ataxy, ataxic; Friedreich's (heredofamilial) (cerebellar) (spinal)
Ataxia, ataxy, ataxic; hereditary; spinal (Friedreich's)
Ataxia, ataxy, ataxic; Hunt's
Ataxia, ataxy, ataxic; spinal; hereditary (Friedreich's)
Ataxia, ataxy, ataxic; spinocerebellar, X-linked recessive
Cardiomyopathy (familial) (idiopathic); due to; Friedreich's ataxia
Disease, diseased; Friedreich's; combined systemic or ataxia
Dyssynergia; cerebellaris myoclonica (Hunt's ataxia)
Friedreich's; ataxia
Friedreich's; combined systemic disease
Friedreich's; sclerosis (cerebellum) (spinal cord)
Hunt's; disease or syndrome (herpetic geniculate ganglionitis); dyssynergia cerebellaris myoclonica
Ramsay-Hunt disease or syndrome; meaning dyssynergia cerebellaris myoclonica
Sclerosis, sclerotic; Friedreich's (spinal cord)
Sclerosis, sclerotic; hereditary; spinal (Friedreich's ataxia)
Sclerosis, sclerotic; spinal (cord) (progressive); hereditary (Friedreich's) (mixed form)