Free Online ICD-9-CM Diagnosis Codes
>
2009
> Diseases Of The Nervous System And Sense Organs
320-389
> Hereditary And Degenerative Diseases Of The Central Nervous System
330-337
> Spinocerebellar disease
334.*
>
2009 ICD-9-CM Diagnosis Code 334.2
Primary cerebellar degeneration
334.1
334.3
334.2 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 334.2:
2010
Also applicable to/known as
Cerebellar ataxia:
Marie's
Sanger-Brown
Dyssynergia cerebellaris myoclonica
Primary cerebellar degeneration:
NOS
hereditary
sporadic
ICD-9-CM Volume 2 Index Entries That Refer To 334.2
Ataxia, ataxy, ataxic
781.3
cerebellar
334.3
hereditary (Marie's)
334.2
family, familial
334.2
cerebral (Marie's)
334.2
spinal (Friedreich's)
334.0
hereditary NEC
334.2
cerebellar
334.2
spastic
334.1
spinal
334.0
heredofamilial (Marie's)
334.2
Marie's (cerebellar) (heredofamilial)
334.2
Sanger-Brown's
334.2
Degeneration, degenerative
cerebellar NEC
334.9
primary (hereditary) (sporadic)
334.2
cortical (cerebellar) (parenchymatous)
334.2
alcoholic
303.9
[
334.4
]
diffuse, due to arteriopathy
437.0
Disease, diseased - see also Syndrome
Hunt's
dyssynergia cerebellaris myoclonica
334.2
Dyssynergia
cerebellaris myoclonica
334.2
Hunt's
syndrome (herpetic geniculate ganglionitis)
053.11
dyssynergia cerebellaris myoclonica
334.2
Marie's
cerebellar ataxia
334.2
Ramsay Hunt syndrome (herpetic geniculate ganglionitis)
053.11
meaning dyssynergia cerebellaris myoclonica
334.2
Sanger-Brown's ataxia
334.2
Sclerosis, sclerotic
brain (general) (lobular)
341.9
hereditary
334.2
hereditary
cerebellar
334.2
Syndrome - see also Disease
Hunt's (herpetic geniculate ganglionitis)
053.11
dyssynergia cerebellaris myoclonica
334.2
Ramsay Hunt's
dyssynergia cerebellaris myoclonica
334.2