G11.3 – Cerebellar ataxia with defective DNA repair
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Tyoe 2 Excludes
Cockayne's syndrome (Q87.19)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
Applicable To
Ataxia telangiectasia [Louis-Bar]
GEM Conversion to ICD-9 CM
Fs: 10000
–
Other spinocerebellar diseases
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
cerebellar
(hereditary)
G11.9
telangiectasia
(Louis-Bar)
G11.3
Ataxia-telangiectasia
(Louis-Bar)
G11.3
Boder-Sedgwick syndrome
(ataxia-telangiectasia)
G11.3
Louis-Bar syndrome
(ataxia-telangiectasia)
G11.3
Syndrome
See also Disease
Telangiectasia, telangiectasis
(verrucous)
I78.1
Sibling Codes
Parent Sibling Codes
View in Tabular
Code | Title |
---|---|
G00-G99 | Diseases of the nervous system (G00-G99) |
G10-G14 | Systemic atrophies primarily affecting the central nervous system (G10-G14) |
G11 | Hereditary ataxia |
G11.3 |
Cerebellar ataxia with defective DNA repair
Type 2 Excludes
Cockayne's syndrome (Q87.19)
other disorders of purine and pyrimidine metabolism (E79.-)
xeroderma pigmentosum (Q82.1)
Applicable to
Ataxia telangiectasia [Louis-Bar]
|